Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Minimum severity
The Philips ALLURA Xper FD10/10 X-ray system may fail to initiate or operate intermittently when using its wired foot switch. Approximately 112 affected units have been distributed in the United States and internationally.
Philips has issued a Class II recall for its ALLURA Xper FD10 operating table due to a wired foot switch defect that may prevent X-ray imaging from initiating or cause intermittent operation.
Medline has recalled 14,379 biopsy valve kits due to complaints about rubber fragments detaching from the valve slit. These fragments could lodge in a patient's airway and may require removal intervention.
Burlington Medical is recalling 961 radiation attenuation caps due to potential degradation of the protective material over time, which could reduce shielding effectiveness.
Burlington Medical has recalled approximately 15,216 Kilt radiation protective garments due to potential degradation of the Xenolite 800 attenuation material, which may reduce protective effectiveness over time.
Intuitive Surgical is recalling 2,095 da Vinci S and Si Tenaculum Forceps Instruments due to increased complaints of frayed or broken pitch cables that could impair instrument function during surgery.
Burlington Medical is recalling BAT (Breast, Axilla and Thyroid) Coverage protective devices due to potential degradation of the attenuation material over time, which may reduce their protective lifespan.
ReCor Medical is recalling the Paradise® Ultrasound Renal Denervation System catheter because a nonconforming product was distributed that should have been scrapped and was not intended for human use.
The Vue Motion V12 cardiac imaging system may display image frames out of sequence during dynamic cine runs. Philips Medical Systems is recalling 3,552 units worldwide due to this potential defect.
Medtronic's MiniMed 700G Insulin Pump malfunctions when elevated or lowered relative to the infusion site, causing unintended insulin over- or under-delivery, which can lead to severe hypoglycemia or hyperglycemia.
Medline is recalling hip surgery kits containing Olympus biopsy valves with a defect that can cause rubber fragments to detach. These fragments pose a risk of lodging in the patient's airway.
Synthes (USA) Products LLC is recalling a surgical screw product due to a manufacturing error where units received incorrect threading. The affected lot may pose a risk if used in orthopedic surgery.
Philips is recalling Azurion 7 B12 X-ray imaging systems due to a wired foot switch defect that may prevent or cause intermittent X-ray image initiation.
Medtronic MiniMed 670G insulin pumps have a defect that may cause over- or under-delivery of insulin based on pump position relative to the infusion site. This can lead to dangerously high or low blood sugar levels.
Appco Pharma LLC is recalling Prazosin Hydrochloride 2mg capsules due to detection of N-nitroso-prazosin impurity above acceptable limits. The recall covers 58,896 bottles distributed nationwide.
K.C. Pharmaceuticals recalls multiple brands of over-the-counter eye drops nationwide due to lack of assurance of sterility. Approximately 315,144 bottles are affected.
GE Healthcare SIGNA Premier MRI scanners may have ferrous steel fittings instead of brass on the magnet rear. During servicing with the magnet powered, technicians could be injured if these fittings are attracted to the magnetic field.
K.C. Pharmaceuticals is recalling 182,424 bottles of Quality Choice and store-brand eye drops nationwide due to lack of sterility assurance in manufacturing. Affected bottles expire May 31, 2026.
K.C. Pharmaceuticals is recalling Quality Choice Moisturizing Relief Eye Drops and related brand variants nationwide due to lack of sterility assurance. Approximately 303,216 bottles may be affected.
Medtronic MiniMed 720G insulin pumps can deliver incorrect insulin doses based on pump position relative to the infusion site, potentially causing severe low or high blood sugar.
Multiple brands of lubricating eye drops manufactured by K.C. Pharmaceuticals have been recalled nationwide due to lack of assurance of sterility. Consumers should stop using affected bottles and consult their healthcare provider if concerned.
Philips is recalling Allura Xper FD10C X-ray imaging systems due to a wired foot switch malfunction that may prevent or intermittently interrupt imaging. The recall affects 15 units distributed across the U.S. and internationally.
GoodSense Eye Drops Original Formula and related store brands are being recalled nationwide due to lack of assurance of sterility. The recall affects 378,144 bottles with specific lot numbers and expiration dates.
Amneal Pharmaceuticals is recalling Tramadol Hydrochloride 50 mg tablets due to a carcinogenic impurity found outside acceptable specifications during testing. The recall affects medication distributed nationwide.
Medtronic's Paradigm insulin pumps may deliver incorrect insulin doses when elevated or lowered relative to the infusion site due to gravitational pressure changes. This can cause severe high or low blood sugar complications.