FDA Warning & Recall Information

On Thursday, the FDA released an announcement regarding Medtronic’s decision to recall two of its devices — the McGrath MAC Video Laryngoscope and the McGrath MAC EMS Video Laryngoscope. Additionally, Medtronic issued updated instructions for the Next-Generation McGrath MAC Video Laryngoscope, which they are not […]

On Thursday, the FDA notified the public of a recall initiated by Abbott Diabetes Care Inc. of three lots of its FreeStyle Libre 3 sensor, which is a component of the company’s FreeStyle Libre 3 Continuous Glucose Monitoring System. The company says that the implicated […]

According to the FDA, Carson City-based company Sierra Stain LLC recalled three shades of water-based tattoo inks from its Bloodline brand due to the presence of high levels of microorganisms. Sierra Stain announced the recall on August 23, 2024. The recall pertains to three shades […]

The FDA recently notified the public of a recall issued by Inari Medical regarding updating instructions for use of its ClotTriever XL Catheter 30mm device after reports of injury and death. The recall does not involve the removal or discontinuation of the product itself, but […]

Almost two weeks ago, the FDA notified the public of Unilever’s recall of eleven lots of its single-serving Popsicle brand Jolly Rancher Frozen Confection Pop products. Unilever attributed the recall to the presence of undeclared milk in the popsicles. The company issued the announcement on […]

The FDA is alerting the public to a recall of cinnamon initiated by Asli Fine Foods of Woodridge, IL. The company announced the recall of one lot of its 7 oz packets of Asli cinnamon powder after detection of lead in the product. Asli Fine […]

According to the FDA, Tandem Diabetes Care, Inc. issued a correction update earlier this month regarding an initial recall issued in March pertaining to the Apple iOS t:connect Mobile App software used with their t:slim X2 insulin pump with Control-IQ technology. The correction does not […]

The FDA alerted the public last Thursday, August 22nd, of a recall involving three lots, or 840 units, of MONTREAL FUDGE produced by Authentik Fudge of Sainte-Julie, Quebec, Canada. The company issued the recall on Wednesday, August 21st, after receiving a complaint from a consumer […]

The FDA has announced an urgent recall of the Defibtech RMU-2000 ARM XR Chest Compression Device due to a motor issue that could render the device inoperable. Defibtech, LLC, initiated the recall on July 12, 2024. Defibtech issued the recall after reports of one injury […]

The FDA announced on Monday, August 26th, a recall initiated by Sunco & Frenchie LLC of two lots of its 10oz Terrafina Golden Raisins due to the potential presence of undeclared sulfites. Consumption of the product could cause a serious and potentially fatal allergic reaction […]

According to the FDA, B. Braun Medical Inc. (B. Braun), of Bethlehem, Pennsylvania, has recalled two lots of its 0.9 Sodium Chloride for Injection USP 1000 mL in E3 containers because the product may contain particulate matter, and its containers may potentially leak fluid. The […]

Perrigo Company plc, of Dubin, Ireland, and Allegan, Michigan, has recalled 16,500 cans of CVS Health and H-E-B Baby-branded Premium Infant Formula with Iron Milk-Based Powder because the product was found to contain an excessive level of Vitamin D, reports the FDA. Initiated by the […]