dvm3609h
FDA notifies veterinarians of animal burn risk linked to human medical devices
Following a recall of grounding pads produced by Megadyne, a machinery industry company, the FDA is notifying veterinarians ...
HME News11h
Urgent recall issued for TrueAire-5 oxygen concentrator
The U.S. Food and Drug Administration has issued an urgent recall for the JMCC5A Ni/TruAire-5 Oxygen Concentrator due to the device spontaneously catching fire.
dermatologyadvisor1d
FDA Alert: Pulmonology Drug Approvals, Recalls, and Device Updates
FDA 2025 pulmonology drug alerts, including drug approvals/warnings, vaccine approvals, and medical device recalls/updates.
FDA Changes Raise Concerns About Food Recalls
The number of hospitalizations and deaths from foodborne illness doubled last year compared to 2023 in the U.S.
Healio6d
FDA recalls Mercury Medical T-piece resuscitator due to ventilation control component
The FDA has recalled Mercury Medical’s Neo-Tee T-Piece Resuscitator, a gas powered resuscitator intended primarily for ...
Amid recalls, Minnesota medtech exec says she was pressured to disregard safety law
Susan Krause of Rosemount alleges New Jersey-based Integra LifeSciences pressured her to lie to regulators. Integra says ...
Olympus Issues Medical Device Advisory Notice to Use Alternative Devices to the MAJ-891 Forceps/Irrigation Plug
Olympus Corporation has announced a voluntary Advisory Notice for the Forceps/Irrigation Plug (Isolated Type) model MAJ-891 related to the risk of device contamination that may result from improper ...
Rethinking Medical Recalls: 3 Ideas For Maximizing Trust
These strategies can create a healthcare ecosystem that prioritizes patient safety, empowers consumers with information and ...
medtechdive10d
FDA webpages on clinical trial diversity removed after Trump orders
The website changes raise concerns about “the interference of politics with the study and the practice” of science and ...
MedPage Today10d
Limbo of Cardiac Device Recalls Has Physicians Ready for Change
A recent study identified 157 cardiovascular devices recalled from 2013 to 2022. Recalls were commonly attributed to device ...
The Cincinnati Enquirer14d
A popular skincare product is part of nationwide FDA recall. Do you have this moisturizer?
The FDA issued a recall for the second-highest recall classification out of three tiers. Here's what we know about why the skin care product was recalled and why. The FDA issued a Class II recall ...