FDA Warning & Recall Information

The FDA recently issued updated recommendations for the GE HealthCare EVair Compressor after testing confirmed safe levels of formaldehyde emissions with use of the device. The update provides a follow up to GE HealthCare’s Urgent Medical Device Correction notice sent to users last year. EVair […]

Concerns about asbestos have prompted the Dynarex Corporation to expand the recall they initiated in late September of Dynacare Baby Powder. According to the FDA, the renewed recall applies to an additional 990 cases of baby powder. The first recall, announced on September 19th, applied to […]

A positive test for Listeria monocytogenes has prompted HH Fresh Trading Corp of California to recall 480 cases of Taiwan Enoki mushrooms. The FDA announced the recall on Saturday, November 2nd. The recall applies to HH Fresh Trading Enoki mushrooms sold at retail stores in […]

The FDA recently notified the public of a recall initiated by the supplement company Boulla LLC of their ZoomMax and ZapMax capsules. The company announced the recall after FDA testing found undisclosed prescription drugs in the supplements. Boulla LLC markets the ZoomMax and ZapMax supplements […]

The discovery of undeclared almond flour has prompted One Roof, LLC., better known as Atwater’s, to recall specific batches of their Spider Web Tarts. The FDA published notice of the recall on October 28, 2024. Atwater’s distributed the tarts on October 19th and 20th at […]

Concerns about nickel exposure have prompted Percussionaire to recall nine lots of their Phasitron 5 breathing circuits. According to the FDA, this is a Class I recall due to risk of serious injury with use of the device. The Phasitron 5 breathing circuit is part […]

Discovery of an undiscovered allergen has prompted R. Walters LLC, known publicly as Elevation Foods, to recall 1,668 units of their Hannaford Seafood Salad. The FDA published notice of the company’s announcement on Thursday, October 31st. Elevation Foods announced the recall after discovering that the […]

According to the FDA, Acme Smoked Fish Corporation is recalling 111 cases of Kirkland Signature Smoked Salmon from Costco stores in Florida. The company initiated the recall after lab testing confirmed the presence of Listeria monocytogenes in a sampling of the product. Acme Smoked Fish Corporation […]

The robotics company Kinova has issued an Urgent Medical Device Correction notice for their Jaco Assistive Robotic Arm due to fire and burn risks. The FDA considers this a Class 1 recall, since continued use of the device without the proposed corrections could cause serious […]

Grand Central Bakery in the Pacific Northwest is recalling several of their frozen pies and pre-made crusts due to the potential presence of undeclared eggs. The FDA published the notice on Saturday, October 26th, just one day after the company’s announcement. The products listed in […]

As a follow-up to a device correction issued several months prior, Hologic, Inc. is now announcing a full product removal of all models of their BioZorb Markers after numerous reports of injury. The FDA is calling this a Class 1 recall. Health care professionals typically […]

Dakota Tom’s Sandwiches out of South Dakota recently issued a voluntary recall of three of their sandwiches in response to a larger national recall involving one of the company’s suppliers. According to the FDA, possible contamination with Listeria monocytogenes is at the center of the recall. […]