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Lexunder is recalling two Food to Live brand organic powders because they may be contaminated with Salmonella. The recall covers 2 products: Organic Moringa Leaf Powder, sold in pouches and bags from 8 oz to 44 lb, and Organic Supergreens Powder Mix, which contains kale and moringa leaf and comes in pouches from 8 oz to 12 lb. About 860 units were affected, and the products were distributed in many U.S. states.

Serious·FDA·Dec 24, 20252 products

Taro Pharmaceuticals is recalling specific lots of Ciclopirox Shampoo 1% because the product failed quality tests for impurities and degradation at the 18-month mark. The affected lots expire January 31, 2026. No injuries have been reported.

Moderate·FDA·Dec 24, 2025

Preferred Pharmaceuticals is recalling ondansetron ODT 4mg tablets because the blister pack containers are not fully sealed, which can cause tablets to fall out. The manufacturer Glenmark Pharmaceuticals notified Preferred Pharmaceuticals of the sealing defect. This affects specific lot numbers distributed nationwide.

Moderate·FDA·Dec 24, 2025

Somerset Therapeutics is recalling three cisatracurium besylate injection products because testing found the drug may be weaker than its label states. The recall covers 10 mg/5 mL, 200 mg/20 mL and 20 mg/10 mL vials, all made by Somerset Therapeutics in India and distributed nationwide. No injuries have been reported.

Moderate·FDA·Dec 24, 2025·Somerset Therapeutics3 products

Golden State Medical Supply's baclofen 10 mg tablets in 1,000-count bottles (Lot GS065762) may contain foreign tablets or capsules mixed in. This affects 2,472 bottles distributed nationwide. No injuries have been reported.

Moderate·FDA·Dec 24, 2025

Novocol is recalling 7 dental anesthetic products because some cartridges may be cracked or broken. The products are sold under names including Xylocaine Dental, Polocaine Dental, Carbocaine, and OraVerse, plus private-label versions from Dentsply, Patterson Dental, darby dental supply, Benco Dental, and Cook-Waite. No injuries have been reported.

Moderate·FDA·Dec 24, 2025·Novocol7 products

Stryker is recalling 2 products: certain MV3 bariatric beds and Arise 1000EX mattresses. The products were sold close together, suggesting they may be used together, but they have not been tested for compatibility and are not designed to be used as a combination.

Moderate·FDA·Dec 17, 20252 products

Datascope is recalling two Cardiosave intra-aortic balloon pump systems, the Cardiosave Hybrid and the Cardiosave Rescue. The recall is for an addendum to the instructions for use that revises the preventative maintenance schedule to match the service manual update made in June 2023. No injuries have been reported.

Moderate·FDA·Dec 17, 20252 products

A screw in certain Nipro Surdial DX hemodialysis systems may loosen or fall out during use. This is a medical device used in dialysis treatment. The affected units have specific serial numbers issued between 2020 and 2024.

Moderate·FDA·Dec 17, 2025

Medline Industries is recalling DEXLOCK Achilles Repair Implant Kits (model MAKT4520, lot 19019) because the drill bit can fuse to the drill guide during surgery. This can delay the procedure while a replacement drill bit and guide are retrieved. No patient injuries have been reported.

Moderate·FDA·Dec 17, 2025

Bard is recalling four InLay Optima ureteral stent kits because the actual stent size may not match the size printed on the label. About 4,700 units are affected, and the kits were distributed in the US and several other countries. No injuries have been reported.

Moderate·FDA·Dec 17, 20254 products

Medline is recalling seven Curad bandage products, including Germ-Shield Touch-Free, Quick Strip, and Fur Friends fabric and plastic bandages. Some packages may have open seals, which could compromise the sterility of the bandages. No injuries have been reported.

Moderate·FDA·Dec 17, 20257 products

Cardinal Health ChemoPlus protective gowns and sleeves have been mislabeled with a five-year shelf life when the actual shelf life is three years. The affected gowns may be used past their true expiration date if the incorrect label is relied upon. No injuries have been reported.

Moderate·FDA·Dec 17, 2025

Orthofix is recalling six spinal implant products, including CONSTRUX, FORZA, Pillar, FIREBIRD and Forza Ti spacer and fusion systems. The FDA says the product labeling contains claims that are not consistently present. No injuries have been reported, and the FDA has not specified a remedy.

FDA·Dec 17, 20256 products

Waldemar Link knee fusion nails in certain lots were shipped with a locking screw installed incorrectly—inserted from the wrong side into the femoral component. This misalignment could affect how the device functions after implantation. Eighteen units were distributed to Alabama, Georgia, and Texas.

Moderate·FDA·Dec 17, 2025

Certain lots of Beckman Coulter Access 2 Reaction Vessels contain small defects on the bottom that may cause errors in laboratory immunoassay instruments. These defects could delay patient test results. The recall affects specific lot numbers distributed nationwide and globally.

Moderate·FDA·Dec 17, 2025

Bard Peripheral Vascular Inc. is recalling Safe-T-Centesis 6 Fr Catheter Drainage Trays because the safety indicator on the catheter may show the wrong position—displaying "sharp" when the catheter is actually "blunt." This could lead medical staff to believe the catheter hasn't entered the body cavity when it actually has, potentially causing discomfort, treatment delays, or injury to organs or blood vessels.

Moderate·FDA·Dec 17, 2025

Medline is recalling specific batches of Medline Perfusion Syringes (model DYNJ39223C) that contain BD Luer Tip Caps. BD's testing found that certain tip cap trays failed biocompatibility tests, meaning the plastic may cause skin irritation, allergic reactions, or other adverse effects if it contacts patients during use. No injuries have been reported so far.

Moderate·FDA·Dec 17, 2025

Some GE Senographe Pristina, Pristina Serena, and Pristina Serena 3D mammography systems were distributed with a missing or incorrect X-ray warning label. This label is required by federal regulation to inform users of radiation hazards. No injuries have been reported.

Moderate·FDA·Dec 17, 2025

Between July 2024 and June 2025, some Philips Azurion R3.0 fluoroscopic X-ray systems (model 722234) were shipped without a required safety spacer. This spacer ensures the X-ray tube maintains a safe distance from patients during standard fluoroscopy procedures, as required by FDA regulations.

Moderate·FDA·Dec 17, 2025

Draeger's ErgoStar CM 40 airway connectors (model MP01840) have developed cracks in the hose during use. This connector is used in breathing systems for mechanically ventilated patients. Multiple complaints have been reported worldwide, and all lot numbers are affected.

Serious·FDA·Dec 17, 20254 products

Defective container - seal not adhering to bottles

FDA·Dec 17, 2025

CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.

FDA·Dec 17, 20253 products

Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.

FDA·Dec 17, 2025·Winder Laboratories

Cross Contamination with Other Products

FDA·Dec 17, 2025

Failed impurities/degradation specifications: out of specification results for Ganirelix acetate acrylic acid adduct impurity.

FDA·Dec 17, 2025

Sub potent drug: during the 9-month stability test conducted, the assay value for the affected lot was below specification limit.

FDA·Dec 17, 2025·Dr. Reddy's

Failed stability specifications: Out of specification for hardness test

FDA·Dec 17, 20252 products

An instrument intended for sequencing DNA libraries with in vitro diagnostic assays is used with reagent kits including flow cells that have flow cell gaskets that have a quality issue, which may lead to flow cell leaks during runs, which could cause run failures, that may result in: No/insufficient data output, instrument fluidics clogs, toxic substance exposure to user.

FDA·Dec 10, 2025·Illumina

Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.

FDA·Dec 10, 2025