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.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Stryker is recalling Sigmoid Notch Radial Plates because the sterile packaging barrier may be compromised during transportation.
Synthes (USA) Products LLC is recalling specific tibial and intramedullary nail wraps because they lack sufficient testing to be considered multi-use items.
Stryker Howmedica Osteonics Corp. is recalling specific rHead, uHead, and other radial implants because their sterile packaging may be compromised by transportation.
C.R. Bard is recalling specific lots of Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters due to a potential breach of the sterile barrier packaging.
C.R. Bard is recalling 37,686 Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters due to a potential breach of the sterile barrier packaging.
Cepheid is recalling Xpert CT/NG Urine Specimen Collection Kits because some lots contain a sub-component with an expiration date earlier than the kit's expiration date.
Getinge Disinfection AB is recalling 20 Model 8666 and 8668 washer/disinfectors due to a potential for unauthenticated remote network access.
Cepheid is recalling Xpert CT/NG Vaginal/Endocervical Specimen Collection Kits because some lots contain a sub-component with an earlier expiration date than the kit itself.
Becton Dickinson & Company is recalling specific lots of BD Vacutainer SST Plus Blood Collection Tubes because some stoppers were manufactured with a reduced cycle cure time.
Invacare is recalling 1,057 Pronto Air power wheelchairs because the batteries may overheat during charging, posing risks of chemical burns and property damage.
Alcon Research, Ltd. is recalling ReSTOR intraocular lenses manufactured for Japan due to reports of post-operative inflammation and toxic anterior segment syndrome (TASS). No US distribution occurred.
Fresenius Medical Care is recalling Naturalyte Liquid Bicarbonate Concentrate due to potential bacterial contamination. The recall covers 2,264,028 units distributed nationwide.
Hitachi Medical Systems America Inc is recalling 173 Oasis Coil Extension Cables used with MRI systems because they may overheat and cause burns.
Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Remel Inc is recalling 1,859 PathoDx Strep Grouping Kits because a reagent may cause weak reactions, potentially leading to failure to identify target species.
B. Braun Interventional Systems is recalling 11 Celsite Implantable Access Port Systems because endotoxin test results were out of specification.
Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Trumpf Medical Systems is recalling 9,287 ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Synthes (USA) Products LLC is recalling 8.5mm Reamer Heads for Flexible Intramedullary Nailing Systems due to the possibility of intraoperative breakage and un-retrieved material fragments.
Etac Supply Center Ab is recalling 13 units of the Etac Relax wall mounted shower seat due to reports of the wall bracket cracking or breaking.
Trumpf Medical Systems is recalling 9,287 surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Trumpf Medical Systems is recalling TruLight 3000/5000 surgical lights because the front joint of the spring arm could break at the monitor interface.
Cadence Inc. is recalling 766 non-sterile Perfectum Tuberculin Glass Syringes because graduation marks are not centered with numeric position marks.
Boston Scientific is recalling 9 AngioJet SOLENT Dista Thrombectomy Sets because they were labeled with an incorrect use-by date of December 2015 instead of November 2015.
Boston Scientific is recalling nine AngioJet Spiroflex Thrombectomy Sets because they were labeled with an incorrect use-by date of December 2015 instead of November 2015.