FDA Warning & Recall Information

On Tuesday, the FDA published a warning related to Zimmer Biomet’s early July recall of its CPT Hip System Femoral Stem 12/14 Neck Taper (CPT Hip System). The FDA cautions patients and healthcare professionals that the updated instructions provided by Zimmer Biomet are likely insufficient […]

The FDA recently warned the public of a recall initiated by Hammond’s Candies of two lots of its Dark Chocolate Filled Mini Waffle Cones due to the potential presence of undeclared milk. The company announced the recall after a customer complained of an allergic reaction […]

On Thursday, the FDA issued a warning regarding the potential for “serious liver injury” in patients taking the medication Veozah (fezolinetant). Along with the warning, the FDA released updated recommendations regarding precautions health care professionals should take when prescribing Veozah and signs and symptoms patients […]

The FDA notified the public Wednesday of a recall initiated by Innovation Bakers, LLC of one lot of its 7-11 Fudge Brownie product. The company attributes the recall to the undeclared presence of walnuts in the brownies. Innovation Bakers announced the decision on Tuesday, September […]

The FDA has authorized the SoClean company to market its SoClean3 device as its most recent product for sanitizing CPAP devices beyond the routine cleaning process outlined in all CPAP instruction manuals. Along with this authorization, the FDA is notifying the public of SoClean’s 2023 […]

According to the FDA, Eagle Produce LLC out of Scottsdale, AZ, is recalling one lot of Kandy-branded whole cantaloupe due to potential contamination with Salmonella. The recall applies to 224 cases of whole cantaloupe distributed and sold between August 13th and August 17th in Michigan, […]

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 […]