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Why Lawsuits Over 'Misleading' Food Labels Are Surging - The New York Times
Class-action litigation against food and beverage companies hit a record high last year, with 220 lawsuits filed in 2020, up from 45 a decade ago, according to a tally by the law firm Perkins Coie.
Labeling Requirements - Misbranding | FDA
Misbranding. Section 502 of the Federal Food, Drug and Cosmetic Act (FFDCA) contains provisions on misbranding including some that relate to false or misleading labeling. A device’s labeling...
What is Misbranding? | False and Misleading Labeling
Misbranding is accidentally or intentionally labeling a product with incorrect information. The error can be innocuous, but it can also cause injury. If you have been harmed by a product due to misbranding, a misbranding product lawyer can potentially help you get compensation for your losses.
21 U.S. Code § 352 - Misbranded drugs and devices
U.S. Code. Notes. prev | next. A drug or device shall be deemed to be misbranded—. (a) False or misleading label. (1) If its labeling is false or misleading in any particular. Health care economic information provided to a payor, formulary committee, or other similar entity with knowledge and expertise in the area of health care economic ...
Misbranding
Misbranding actions strike at some of the most closely held constitutional rights. Limitations on labeling impact both a facility’s First Amendment right to free speech and the consumers freedom of choice. Constitutional rights stand in equal, if not greater, importance to the FDA’s statutory mission to protect the public from fraudulent ...
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