FDA Warning & Recall Information

A Class I Medical Device Correction (MDC) sent to hospitals on December 8, 2023, regarding the intended use of Megadyne’s Mega Soft Universal and Universal Plus Reusable Patient Return Electrodes was revised by Megadyne on February 29, 2024, according to the FDA. Officials said that […]

Apopka, Florida-based El Chilar Rodriguez LLC has voluntarily recalled 127 cases (12 1.25-ounce bags/case) of its El Chilar Ground Cinnamon “Canela Molida” because the product may contain traces of lead at elevated levels, according to the FDA. While exposure to lead at very low levels […]

Par Pharmaceutical, Inc. (Par), one of the operating companies of Endo International, announced has recalled one lot of its 20 mg/20mL (1mg/mL) Treprostinil Injection because the product solution may contain silicone particulates, according to the FDA. Officials warn that administering an injectable product with foreign […]

La Mirada, California-based La Fiesta Food Products has recalled its .87-ounce Cinnamon Ground because the product may contain a lead contaminant, according to the FDA. Consumers should note that while lead is a toxic substance, it is found in trace amounts throughout our environment, and […]

According to the FDA, Vyaire Medical, Inc. has recalled nine (9) AirLife Adult Manual Resuscitators because the products were found to have a manufacturing defect that poses a risk of serious injuries or death to its users. Initiated by the company on December 6, 2023, […]

Ellison Bay, Wisconsin-based Kick Ash Products has recalled a single lot (#061241) of its Door County Love Dark Chocolate Cherry Granola because the product contains almonds, a major allergen not declared in the ingredient list on its label, reports the FDA. Individuals who live with […]

According to the FDA, a number of production lots of Trader Joe’s Nuts – 50% Less Sodium Roasted & Salted Whole Cashews – has been recalled by Wenders LLC, of Dublin, California, due to concerns of a possible Salmonella contamination. While healthy individuals who become […]

Patients and healthcare providers are advised of a Class I recall of Abbott’s HeartMate Touch System (version 1.0.32) due to the potential for unexpected stops and starts in its pump, which could lead to serious injuries or death, according to the FDA. Officials say 1,560 […]

John B. Sanfilippo & Son, Inc (JBSS), of Elgin, Illinois, has recalled a limited quantity of its 8.25-ounce Great Value Honey Roasted Cashews because the product may contain traces of coconut and milk, two major allergens that do not appear on its ingredient list. Individuals […]

Garden Grove, California-based LQNN, Inc., has recalled its Banh Ba Xa and several varieties of its Banh Pia, under multiple lot numbers and best-by dates, due to the potential presence of egg, an ingredient not declared on the product label. Individuals who live with an […]

Muskegon, Michigan-based Wesco, Inc. has recalled 750 units of its Wesco Mint No Bake Cookie Bites because it may contain traces of peanut, a major allergen not listed in the product’s ingredient list, according to the FDA. Individuals who live with a peanut allergy or […]

Following reports of adverse events linked to electrical operating room tables, the U.S. Food and Drug Administration (FDA) is emphasizing user training and advising healthcare providers to carefully follow instructions in the manufacturer’s product manual to mitigate risks to patients. Indicated to properly position a […]