On June 1, 2017, the Mandatory Initial Discovery Pilot Project (MIDP) took effect in the Northern District of Illinois. With only limited exceptions, the MIDP applies to all cases filed after June 1 and significantly impacts how cases in the Northern District of Illinois will proceed. In particular, cases in which defendants are seeking to dismiss a complaint or which involve large amounts of discovery will be most affected by the changes. Only a few types of cases are exempt from the MIDP: (a) cases exempted from initial disclosures by Rule 26(a)(1)(B); (b) cases transferred for consolidated administration by the Judicial Panel on Multidistrict Litigation; (c) patent cases; and (d) actions under the Private Securities Litigation Reform Act.
As readers of this blog know, we have been closely following developments regarding claims for medical monitoring. (Medical Monitoring Claims in Illinois, Part 1; Medical Monitoring Claims in Illinois, Part 2.) A recent decision arising out of Hoosick Falls, New York, allowed Plaintiffs’ request for a medical monitoring fund to survive defendants’ motion to dismiss. On Feb. 24, 2016, Plaintiffs, on behalf of a putative class, brought suit against Saint-Gobain Performance Plastics Corp. and Honeywell International Inc., alleging that Defendants’ manufacturing facilities in the Village of Hoosick Falls, New York, caused groundwater contamination. Specifically, Plaintiffs alleged that Defendants’ manufacturing and disposal of products containing perfluorooctanoic acid (PFOA) caused PFOA to contaminate the municipal water system and private wells. PFOA is a chemical used to create water, oil, and grease repellency which can remain in soil and water for extended periods of time. Plaintiffs alleged that they experienced heightened blood levels of PFOA, which may cause cancer, as well as loss of property value due to the stigma of contaminated groundwater. The complaint asserted claims for negligence, private nuisance, trespass, and strict liability for abnormally dangerous activity. The complaint set forth two subclasses of plaintiffs based on their water source: (1) Municipal Water Property Damage – owners of real property in the village who receive drinking water from the municipal water supply; and (2) Private Well Water Property Damage – owners of real property in the village who receive drinking water from a privately-owned well.
Defendants brought a motion to dismiss for failure to state a claim. Significantly, Plaintiffs sought to establish a medical monitoring program designed to fund future testing and treatment for diseases related to PFOA exposure. Defendants argued that Plaintiffs asserted a separate medical monitoring claim without alleging the existence of present physical injuries, a requisite under New York law. The Court disagreed, finding that Plaintiffs properly alleged an injury to both person and property. In particular, the Court adopted the reasoning of the Second Circuit in In re World Trade Ctr. Lower Manhattan Disaster Site Litig., holding that the heightened accumulation of PFOA in Plaintiffs’ blood levels permits a claim for negligence seeking medical monitoring damages. See 758 F. 3d 202, 213 (2nd Cir. 2014). Even if the accumulation of toxins in blood were not a sufficient injury, the Court relied on Caronia v. Philip Morris USA, Inc. to find that plaintiffs may seek medical monitoring as consequential damages for a tort alleging injury to property. 2011 WL 338425 (E.D.N.Y. Jan. 13, 2011) aff’d in part, question certified, 715 F.3d 417 (2d Cir. 2013), certified question accepted, 21 N.Y.3d 937 (2013), and certified question answered, 22 N.Y.3d 439 (2013), and aff’d, 748 F.3d 454 (2d Cir. 2014). However, the Court cautioned that the decision did not determine what Plaintiffs must prove at trial to recover consequential medical monitoring damages. Noting that the Defendants’ motion to dismiss raised “several complex and novel issues of New York law” which is “significantly muddled,” the Court certified the question for interlocutory appeal. We will continue to follow this appeal closely.
Defendants also argued that the property damage claims based on injury to groundwater must be dismissed because the water is a public resource belonging to the state of New York, not individual residents. The Court agreed that Plaintiffs could not state a claim for relief if the only alleged injury was to the public groundwater; however, the Court found that Plaintiffs’ claims for negligence and strict liability based on property damage survived because they alleged the loss of their potable water, reduction in property value, and sought damages for remediation costs for property contamination and restoring their potable water supply. Defendants moved to dismiss the trespass claim brought by the Private Well Plaintiffs on the basis that the Plaintiffs’ property was not injured by PFOA contamination. The Court rejected this argument, finding that the groundwater provided the medium through which the contamination moved into Plaintiffs’ private wells, thus injuring Plaintiffs’ private property. Defendants also moved to dismiss the private nuisance claim for failure to state a claim. Defendants argued that a private nuisance claim must affect only a small number of people, but Plaintiffs alleged a widespread injury. The Court agreed in part and dismissed the Municipal Water Plaintiffs’ nuisance claim, finding that the allegations of harm suffered by “all renters and owners in Hoosick Falls” constituted a public nuisance, which only the state of its subdivision have standing to bring; however, the Private Well Plaintiffs suffered a “special loss” sufficient to maintain a private nuisance action where they had to install point of entry treatment systems on their property which requires ongoing maintenance. Because of this, the Court allowed the Private Well Plaintiffs’ nuisance claim to proceed.
California’s Century City Bar Association (CCBA) recently selected GT Century City shareholder Robert J. Herrington, Co-Chair of the global law firm’s Products Liability and Mass Torts Practice, as the 2017 Class Action Litigation Lawyer of the Year. Herrington was honored at the Association’s 49th Annual Installation Banquet and Awards Ceremony at the Intercontinental Hotel, Century City on March 30, 2017.
The CCBA notes that its mission is to provide top-quality legal education; enhance and promote the sense of community among Century City lawyers; honor Century City lawyers who have achieved extraordinary accomplishments; and to provide leadership opportunities to lawyers who participate in the CCBA.
Herrington serves as Co-Chair of the firm’s Products Liability & Mass Torts Practice. A first-chair trial litigator, he has broad experience defending major corporations in class actions and product liability law suits. This includes in the areas of false advertising, unfair competition, product defect, and privacy. Committed to raising awareness of class action litigation risk, Herrington is the author of the best-selling book, Verdict for the Defense (Sutton Hart Press 2011), and a co-author of The Class Action Fairness Act: Law and Strategy (ABA Publishing 2013). Herrington was previously on Law360‘s list of “Top Attorneys Under 40” for Class Actions and is ranked for his work in Product Liability, Mass Tort and Class Action: Consumer Products by The Legal 500. He is a member of the American Bar Association’s Litigation Section’s Appellate Practice Committee, as well as its Class Action and Derivative Suits Committee and serves as Co-Editor of the associated newsletter.
In honoring Rob, the CCBA prepared this video which provides excellent insight into his practice and motivations for the top tier service he provides GT’s clients.
For more details, please click here.
The environmental parameters associated with textiles continue to attract both regulatory and value chain attention. In an interesting development, Vietnam just relaxed its chemical testing rules for exported textiles (e.g., textiles and apparel exported to the U.S. and EU markets), specifically for formaldehyde and aromatic amines. Formaldehyde is frequently used in treating textiles, including popular “no-iron” and “permanent press” textiles. Aromatic amines are present in some common dyes used in textiles and include chemicals that are either known or suspected to be carcinogens.
The presence of these chemicals in textiles is relatively unregulated at the federal level in the United States, though there has been some attention at the state level. For example, formaldehyde is subject to California’s Proposition 65, and some crafts/textile stores in California post Proposition 65 warnings for their imported textiles. Washington, Maine, and Minnesota have statutes with reporting requirements for what are typically described as “high priority” chemicals, including formaldehyde, intentionally added to children’s products (though not all of these encompass apparel). There has been occasional litigation based on claims of skin irritation allegedly caused by the presence of formaldehyde in apparel.
Perhaps more importantly than formal regulation, the chemical content of apparel, including formaldehyde, receives a certain amount of attention in social media. This reverberates into market impacts, with some companies trying to leverage this into a competitive advantage by advertising “chemical-free” clothing. This leverage could increase if major buyers begin to drive chemical content requirements through their value chains. Some of the most prominent retailers, including Walmart, have already launched initiatives to decrease or remove certain chemicals, including formaldehyde, from a range of products, including personal care, cosmetics and cleaning products. Some major buyers and brands, including Walmart, Levi Strauss, and VF have signed on to policies and standards associated with sustainable forestry and agriculture that affect the value chain for a variety of raw materials for textiles, including rayon and cotton.
Decisions by Vietnam to impose more stringent chemical content standards for apparel on its own market than it does for its strong apparel export market might increase public and retailer attention to this issue. The most likely ongoing pressure points will probably be from social media, consumers, and companies seeking to leverage this issue for competitive advantage. And even if increased federal regulation is viewed by some as less likely under the current administration, that will not restrict state regulators from taking action (the preemption provisions of the newly amended Toxic Substances Control Act will operate, roughly speaking, in inverse proportion to the degree of EPA regulation of specific chemicals: the less active EPA is, the more freedom of movement at the state level).
In our last post, we discussed Illinois Appellate Court decisions concerning medical monitoring claims. Plaintiffs have been similarly unsuccessful at the trial court level. Judge Leroy Martin in the Circuit Court of Cook County (Chancery) dismissed a medical monitoring claim pursuant to defendants’ 735 ILCS 5/2-615 motion to dismiss. See Pierscionek v. Ill. High Sch. Ass’n, 2015 Ill. Cir. LEXIS 24 (Ill. Cir. Ct. October 27, 2015). The court likened plaintiff’s claim for medical monitoring to Lewis I and dismissed the complaint:
The court in Lewis was concerned with some of the same issues presented in the case at bar—a plaintiff who fails to allege the existence of a present injury and the fundamental difference between a claim seeking damages for an increased risk of future harm and one that seeks compensation for the cost of medical examinations. Ultimately, the Lewis decision determined that plaintiffs had failed to plead tort claims because they failed to establish a causative link between the tortious acts of a specific defendant and damages sought — the cost of screening for lead poisoning….The complaint before this court seeks ongoing medical monitoring as opposed to screening for a medical condition but the pleading fails to establish a causative link between IHSA and the damages sought.
The opinion further stated, unequivocally, “Illinois law does not recognize a medical-monitoring-only cause of action.” Pierscionek, 2015 Ill. Cir. LEXIS 24, *11 (Ill. Cir. Ct. Oct. 27, 2015).
In furtherance of the Jensen court’s admonishment that that Lewis I does not support the viability of medical monitoring only claims, the Illinois Appellate Court has also supported the rejection of such claims. See Campbell v. A.C. Equip. Serv. Corp., Inc., 242 Ill. App. 3d 707 (4th Dist. 1993) (where the court did not recognize a cause of action to recover expenses for medical monitoring absent present physical injury); Betts v. Manville Personal Injury Settlement Trust, 224 Ill. App. 3d 882 (4th Dist. 1992) (where the court rejected medical monitoring damages in an asbestos case absent proof of present injury).
While the Illinois Supreme Court has not yet recognized this type of claim, several federal district court opinions have concluded that Illinois would recognize independent claims for medical monitoring. Stella v. LVMH Perfumes & Cosmetics USA, Inc., 564 F. Supp.2d 833, 836 (N.D. Ill. 2008); Gates v. Rohm & Haas Co., 2007 WL 2155665, at *4-5 (E.D. Pa. July 26, 2007) (applying Illinois law); Muniz v. Rexnord Corp., 2006 WL 1519571, at *6-7 (N.D. Ill. 2006); Carey v. Kerr-McGee Chemical Corp., 999 F. Supp. 1109, 1119 (N.D. Ill. 1998)(predicting that the Illinois Supreme Court would uphold a claim for medical monitoring without requiring plaintiffs to plead and prove a present physical injury).
If the Illinois Supreme Court allows medical monitoring claims for plaintiffs without a present physical injury, the court should provide instructions for how a defendant can establish and manage a fund for medical monitoring. Such questions include whether a defendant must monitor for other medical issues, time limitations, administrative authority, size of fund, and adapting to increased costs of health care. Without guidance as to these fundamental issues, the courts may be faced with increased litigation over the proper way for a defendant to establish and manage a medical monitoring fund.
On March 31, 2017, the D.C. Circuit held that the Federal Communications Commission (FCC) lacked authority under the Telephone Consumer Protection Act, as amended by the Junk Fax Prevention Act (collectively, the TCPA), to issue a rule, known as the “Solicited Fax Rule,” requiring businesses to include opt-out notices on solicited fax advertisements. Bais Yaakov of Spring Valley, et. Al. v. Federal Communications Commission and United States of America, No. 14-1234 (D.C. Cir. Mar. 31, 2017). Following this ruling, FCC Chairman Ajit Pai issued a statement praising the ruling, reiterating his earlier criticism that the FCC’s approach to interpreting the law in the Solicited Fax Rule reflected “convoluted gymnastics.” The decision in Bais Yaakov and Chairman Pai’s statement may have implications beyond the Solicited Fax Rule, as other FCC interpretations of the TCPA arguably deviate from the statutory text in a manner similar to the Solicited Fax Rule. Accordingly, Bais Yaakov may signal an opportunity for TCPA defendants to pursue new challenges to the FCC’s rulemaking authority in opposition to questionable agency interpretations.
Medical monitoring has yet to gain traction in Illinois. Plaintiffs with medical monitoring only claims – seeking future testing to determine whether defendants’ alleged negligence has caused the injuries feared – have been unsuccessful in Illinois. Although the Illinois Supreme Court has not ruled specifically on medical monitoring, existing Illinois law does not allow for medical monitoring absent a present physical injury.
The Illinois appellate court first explored a remedy for medical monitoring without proof of present physical injury in Lewis v. Lead Industries Ass’n (793 N.E. 2d 869 (Ill. App. Ct. 2003) (Lewis I). The Lewis plaintiffs sought to recover damages for defendants’ alleged manufacture, distribution, and promotion of paint containing lead. The Lewis case was dismissed for failure to state a claim, but the plaintiffs appealed the dismissal. On appeal, the court accepted the plaintiffs’ theory that the cost of lead testing or assessment could constitute compensable damage, but held that plaintiffs failed to state a claim because they had not adequately pled the requisite causation element. The plaintiffs argued that the complaint contained causation allegations because they had alleged that “the risk of poisoning from exposure to lead pigments in paint such as that promoted and supplied by the defendants is so significant that it has become medically necessary that all children six months through six years of age residing in the State of Illinois be tested” under the Lead Poisoning Prevention Act (410 ILCS 45/1 et seq. (West 2000)). The court disagreed, holding that the plaintiffs had failed to identify a specific manufacturer and therefore failed to allege the required causal link between a specific defendant’s acts and the plaintiff’s injuries. The appellate court reversed the decision in part, but did not reject medical monitoring absent physical injury. See Lewis v. NL Indus., 2013 IL App (1st) 122080 (Lewis II). However, in Jensen v. Bayer AG, the court found that the plaintiff’s claim for medical monitoring for potential future harm, where no present injury is shown, could not proceed. 371 Ill. App. 3d 682, 693 (1st Dist. 2007). The Jensen plaintiffs brought a claim for medical monitoring without alleging a present injury, arguing that taking medication for cholesterol increased their risk of developing a disease in the future. In response to plaintiffs’ reliance on Lewis I, the court stated that Lewis I did not address whether a plaintiff may bring a claim for medical monitoring for potential future harm where plaintiff does not allege a present injury. The Jensen court further cautioned that Lewis did not provide trial courts with guidance on the elements necessary to state an independent claim for medical monitoring absent present injury.
In HPF, L.L.C. v. Gen. Star Indem. Co., 338 Ill. App. 3d 912, 913 (1st Dist. 2003), the court examined the duty to defend suits for medical monitoring. The insured was a distributor of herbal dietary supplements (Herbal Phen-Fen) marketed as safe and effective treatments for obesity. The insured’s policy provided coverage for “those sums that the insured becomes legally obligated to pay as damages because of ‘bodily injury’ or ‘property damage’ to which this insurance applies.” Id. at 916. The underlying complaint sought an injunction against the insured based on misleading marketing and unlawful distribution of an alleged ineffective supplement. The complaint did not seek damages based on bodily injury, but, in the prayer for relief, sought to establish a medical monitoring fund for users of Herbal Phen-Fen to test for future negative health effects. Absent allegations of bodily injury to plaintiffs, the insurance carrier denied that it had a duty to defend or indemnify the insured. The court agreed, finding that the underlying complaint did not seek damages for bodily injury and did not fall within the insured’s coverage policy. Id. at 918.
The most recent case involving medical monitoring before the Illinois Appellate Court was dismissed due to a statute of limitations issue. See Allen v. YRC Worldwide Inc., 2015 IL App (1st) 143053. Defendants filed a 2-619.1 motion to dismiss plaintiffs’ complaint alleging the defendants were responsible for contaminating the village water supply with vinyl chloride. Defendants’ 2-615 motion sought to dismiss the claim for failure to state a cause of action for medical monitoring, while Defendants’ 2-619 motion sought dismissal based on statute of limitations. The plaintiffs’ complaint requested that defendants fund periodic medical monitoring for plaintiffs to determine whether plaintiffs were suffering from any of the increased risks associated with vinyl chloride. The Allen court found that the statute of limitations was not tolled and barred Plaintiffs’ medical monitoring claim against defendants for allegedly contaminating residents’ water supply. Based on this finding, the court did not determine whether the plaintiffs stated a claim for medical monitoring.
To read Part 2, click here.
On Tuesday, April 4, 2017, at 1:00 pm ET, Greenberg Traurig Attorneys Anthony Cortez and Greg Sperla will be presenting a webinar hosted by AudioSolutionz entitled “Proposition 65 – Hot Topics and Recent Developments Affecting Consumer Product Companies.” This webinar will assist attendees to better understand the Impact of Proposition 65 on retail business and get practical strategies for compliance.
Proposition 65 now covers all industries doing business in California, but retail and CPG are in the crosshairs. To make matters worse, 2017 is likely to bring more litigation. Taking steps now to avoid a lawsuit could save thousands later on. This session will help participants to understand what changes have occurred and what potential costly proposals are in the works. Guidance will be given on Prop. 65, and practical examples of real-life scenarios will be discussed.
Session highlights will include:
- Proposition 65 covers nearly every retail and CPG company doing business in California
- Consumer product businesses hit hard in recent years, but 2017 could be worse
- Major changes to Proposition 65 warnings adopted in 2016, but compliance should start now
- Retailers have a wide variety of new obligations and compliance options
- New chemicals listed in 2015 will result in even more litigation in 2017
- New litigation trends in 2017 mean potentially more lawsuits for retail/CPG
Anyone interested in registering can do so here. You may apply coupon code “PROP40” to get $40 off at checkout.
Greenberg Traurig’s Food & Beverage practice group recently gave a very well-attended presentation at the world’s largest natural, organic, and healthy products show of the year in Anaheim, California, Natural Products ExpoWest. The presentation, entitled “All Natural to Zero Calories: The A to Z of Claims,” addressed claims made for products in the food and beverages category, and the effects these claims can have on a variety of areas. Justin Prochnow, a shareholder in GT’s Denver office, kicked off the presentation, discussing the regulation of claims used in labeling and advertising, as well as some of the claims that have been frequently targeted by class action plaintiffs lawyers. Rick Shackelford, Los Angeles shareholder and co-chair of GT’s Class Action practice group, followed with a discussion about some of the recent class action lawsuits in the sector and what to do when presented with a demand letter or Complaint from a plaintiff’s lawyer. Anthony Cortez, a shareholder in the Sacramento office, next talked about Proposition 65 issues affecting the food, beverage, and supplement industries, including the disclosure of BPA in packaging. Finally, Ed Schultz, a Corporate practice shareholder in the Los Angeles office, provided some insights on factors that private equity groups and other investors might be looking at when investing in food and beverage businesses and considerations for owners looking to raise funds or sell their company. The result was a great opportunity to provide some valuable insights as well as outline the depth of experience and range of services that GT attorneys can provide to companies in the food, beverage, and supplement industries. Please do not hesitate to reach out to any of the GT attorneys who were involved in the panel discussion with questions related to the food and beverage sector.
In Briseno v. ConAgra Foods, Inc., ___ F.3d ___ (9th Cir. Jan. 3, 2017), the Ninth Circuit held that Rule 23 does not require plaintiffs to establish an “administratively feasible” means of identifying putative class members, expressly rejecting decisions like Carrera v. Bayer Corp., 727 F.3d 300, 306-08 (3d Cir. 2013). But the decision goes well beyond administrative feasibility. Plaintiffs counsel will argue that the decision also endorses aggregate liability and damages determinations in consumer fraud cases to be followed by a “claims process” overseen by claims administrators. The impact of the decision remains to be seen, but Briseno is bad news for class action defendants, as it likely will make class certification easier in the Ninth Circuit. This article discusses the Briseno decision and offers key takeaways for future cases.
The Ninth Circuit’s Briseno Decision
The Briseno case is one of many class actions challenging food labels. These cases have become substantially more popular in the plaintiffs’ bar, because they do not usually present any opportunity for defendants to move them into arbitration based on class action waivers in arbitration agreements. Customers who buy off the shelf do not agree to arbitrate their claims.
The Briseno plaintiffs claim that a “100% Natural” label is false or misleading because Wesson oils are made from bioengineered ingredients, which the plaintiffs argue are not “natural.”