FDA warns patients to stop using six lots of compounded injections
The FDA posted a nationwide recall of six Centric Compounding injection lots after the company reported elevated endotoxin levels and nine reaction reports.
The FDA posted a nationwide recall of six Centric Compounding injection lots after the company reported elevated endotoxin levels and nine reaction reports.
The FDA says hospitals should inspect Draeger VentStar Resus Neo circuits for cracked or detached hoses before use and discard damaged units.
The Fifth Circuit heard Louisiana’s challenge to telehealth mifepristone access, but FDA rules remain in place while the appeal proceeds.
FDA classified a nationwide Luna G3 APAP recall after firmware may trigger shutdowns under specific conditions. Patients should check their device.
Federal officials are investigating 22 Salmonella cases linked to recalled broccoli sprouts from an Idaho grower sold in Idaho, Montana and Washington.
CDC ended a record Cyclospora outbreak linked to recalled iceberg lettuce, but FDA testing and root-cause work continue as broader U.S. cases remain high.
A Sept. 11 FDA update confirms recalled frozen berries reached Walmart and Publix stores across 27 states and Puerto Rico. Operators should check stock and sanitize equipment.
FDA says two Northwest Naturals raw pet-food lots sold nationwide tested positive for Salmonella and Listeria. Here is what pet owners should do now.
FDA lists 84 illnesses in a Salmonella Newport investigation posted August 26, but no food, recall or product-specific consumer warning has been identified.
The FDA would require notices for many ingredients claimed to be generally recognized as safe, but the proposal would not create blanket preapproval.
The FDA authorized three JUUL2 products for lawful U.S. marketing, while stressing that the decision is not a safety endorsement or quit-smoking approval.
FDA reports 431 illnesses in 32 states in an ongoing Salmonella investigation linked to recalled jalapeños, with restaurant and prepared-food recalls expanding.
The FDA approved weekly Mimrylo for adults with poorly controlled polycythemia vera, offering a new way to reduce phlebotomies while requiring close blood-count monitoring.
Trump’s FDA nominee Heidi Overton still needs Senate confirmation while Kyle Diamantas remains acting commissioner and the FDA lists key vacancies and acting posts.
The FDA and CDC added Georgia, Tennessee and Texas to a recalled-lettuce outbreak with 11,458 illnesses, 495 hospitalizations and two deaths.
Baxter is voluntarily recalling one U.S. lot of citrate solution used with automated apheresis devices. Facilities should stop use, quarantine units and arrange returns.
The FDA has finalized removal of an abandoned sausage-casing color authorization while weighing a separate proposal affecting orange skins.
The FDA identified iceberg lettuce as the leading food item of interest in a Cyclospora investigation and listed eight states in the distribution footprint of a Taylor Farms de Mexico recall.
The FDA says Taylor Farms de Mexico was the common supplier of shredded iceberg lettuce served at Taco Bell locations where people later became ill. The investigation remains ongoing, and no positive product sample had been confirmed as of July 19.
The FDA opened an outbreak investigation after Midwest Poultry Services recalled white-shell and brown cage-free eggs with sell-by or best-by dates from July 20 through Aug. 17, 2026.
Federal officials remain focused on Taylor Farms lettuce as a possible source of a multistate cyclospora outbreak, even after an initially positive sample was found to be inaccurate.
The FDA says Boston Scientific has opened a worldwide correction for software used in certain ACCOLADE-family pacemakers and CRT-P devices.