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
Philips ALLURA Xper FD20 biplane X-ray systems may fail to initiate imaging or operate intermittently when using the wired foot switch. A total of 461 units were affected.
Synthes recalled 77 units of VOLT Locking Screw Tap due to a manufacturing error where the wrong product lot was shipped, resulting in incorrect thread dimensions.
Philips is recalling Allura Xper medical imaging systems due to wired foot switch failures that may prevent X-ray imaging from initiating or cause intermittent operation. No injuries have been reported, but affected units should be checked immediately.
Medtronic MiniMed Paradigm insulin pumps (MMT-712, MMT-715) can deliver too much or too little insulin when the pump is positioned higher or lower than the injection site, causing severe low or high blood sugar.
Medline is recalling 651,789 ENFIT G-Tube Connectors because they may not form a proper seal with compatible feeding devices, risking leakage that could delay care and cause fluid loss.
Civco Medical Instruments is recalling the eTRAX Needle System Starter Kit 16G for Aurora Trackers due to an inspection and programming error that may cause the needle tip position to be incorrectly identified on the user interface.
Oxoid's Microbact 12L Listeria Identification Kit (lot 4494873) may provide incorrect organism identification results due to ambiguous color reactions in test wells. Two kits were distributed nationwide in Georgia and California.
Burlington Medical recalls Demi Half Aprons due to potential degradation of Xenolite 800 radiation-shielding material over time. The recall affects 29 units manufactured between January 16, 2025, and January 21, 2026.
Philips has identified a foot-switch malfunction on ALLURA Xper FD10F X-ray systems that may prevent imaging from starting or cause intermittent operation. The defect affects 10 systems and risks delaying diagnostic procedures.
Siemens is recalling Atellica CH A1c test kits that may produce depressed results when used with RCRP on the same analyzer. This could delay diabetes diagnosis or result in inadequate treatment decisions.
Medline recalls 9,040 ENFIT G-tube connector kits due to manufacturing defects preventing proper sealing and causing leakage, risking delayed care. Over-tightening to prevent leakage risks infection and additional clinical complications.
Burlington Medical is recalling Protective Sleeves due to potential attenuation material degradation. The issue affects approximately 1,129 units distributed worldwide.
Intuitive Surgical is recalling da Vinci S and Si Grasping Retractor surgical instruments due to increased reports of broken or frayed grip cables. Approximately 2,660 affected units have been distributed worldwide.
Civco is recalling eTRAX Needle Sensors due to a programming error that could cause the needle tip position to be incorrectly identified on the user interface.
The Azurion 7 M12 X-ray imaging system may fail to initiate imaging or may operate intermittently due to a wired foot switch malfunction. No patient injuries have been reported.
Philips Azurion 3 M15 X-ray imaging systems are being recalled because the wired foot switch malfunction may prevent X-ray imaging from initiating or cause imaging to occur intermittently. Approximately 798 units have been distributed in the United States and internationally.
The eTRAX Needle System Starter Kit 12G contains a programming error in its needle sensor that can cause incorrect needle tip position display on the user interface. Civco Medical Instruments is recalling affected units.
Medtronic MiniMed 630G insulin pumps may deliver incorrect insulin doses when elevated or lowered relative to the infusion site, potentially causing severe hypoglycemia, seizures, or death.
Mentor Texas is recalling Artoura Breast Tissue Expanders because their infusion sets contain dull or blunt needle tips that may be difficult to advance and may break during use.
The Philips Allura Xper FD20/15 X-ray imaging system may fail to initiate or may initiate intermittently when using the wired foot switch. Philips is recalling 296 affected units (68 in the US, 228 internationally) to address this functional defect.
Stryker surgical light assemblies may not adequately support the ceiling cover weight, creating a fall risk. The Class II recall affects 6,170 units distributed worldwide.
Philips is recalling 111 Allura Xper FD20/20 X-ray imaging systems due to a wired foot switch defect that may prevent imaging from being initiated or cause intermittent operation.
The ALLURA Xper FD10 X-ray imaging system may fail to initiate imaging or operate intermittently when using the wired foot switch. A total of 2,291 units are affected.
Cardinal Health is recalling 198,900 units of Monoject Tuberculin Syringes because packages labeled as Tuberculin Syringes contain U-100 Insulin syringes instead. This mislabeling could lead to dosing or injection errors.
Volkswagen is recalling certain 2024 and 2023 ID.4 vehicles due to loose fasteners on the passenger-side frontal air bag inflator. An improperly secured inflator may not deploy as intended during a crash.