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
Berchtold Corp. is recalling 17 Chromovision HD Wireless Cameras because loose wire connections may cause image distortion or loss during surgical procedures.
Sunrise Medical is recalling 14,035 Padded Swing Away Arm Rests for specific wheelchair models because reports indicate injury when the armrest is used to support full body weight.
Smiths Medical is recalling Medfusion 4000 Syringe Infusion Pumps due to a software anomaly that causes device history log corruption and triggers a Watchdog Fail-Safe alarm.
Zimmer Inc. is recalling Nextgen Complete Knee Solution replacement jaws because the spring clip may fracture or fall off during use, potentially leaving fragments in the surgical site.
Zimmer Inc. is recalling 1,662 Nextgen Complete Knee Solution Femoral and Provisional Impactor/Extractor instruments because the spring clip may fracture or fall off during use, potentially leaving fragments in the surgical site.
ICU Medical is recalling 4,625 High Pressure Stopcocks because a molding defect may cause side ports to become totally occluded.
GE OEC Medical Systems is recalling OEC 9800 Plus Digital imaging systems due to a hard disk drive issue. The recall covers 82 units distributed worldwide.
Intuitive Surgical is recalling specific lots of Instrument Arm Drapes because the sterile adaptor may have difficulty engaging an instrument during surgery.
Church & Dwight is recalling Spinbrush Pro Whitening toothbrushes due to a potential small parts choking hazard if used beyond the recommended 3-month brush head life.
Church & Dwight is recalling Spinbrush Pro White Sonic Crest Powered Toothbrushes due to a potential small parts choking hazard if used beyond the recommended 3-month brush head life.
Intuitive Surgical is recalling specific lots of da Vinci Instrument Arm Drapes because the sterile adaptor may have difficulty engaging an instrument.
Church & Dwight is recalling Arm and Hammer Spinbrush Pro Clean Sonic toothbrushes due to a small parts choking hazard if brush heads are used beyond their recommended life.
Integra LifeSciences is recalling Advansys Medial Lisfranc Plates because an incorrect surgical technique may cause potential rupture of the tibialis anterior tendon.
Church & Dwight is recalling Arm and Hammer Spinbrush ProClean Sonic Recharge units due to a potential choking hazard from small parts if used beyond the recommended brush head life.
Stryker is recalling 210 RF Cannula units because 5mm and 10mm needles were mistakenly packaged in the wrong boxes. This error could lead to thermal skin lesions if the larger tip is used in cervical procedures.
Perkinelmer is recalling 78 Genetic Screening Processor units worldwide because shaker unit contamination causes decreased signal activity in neonatal screening assays.
Church & Dwight is recalling Arm and Hammer Spinbrush Pro White Sonic Toothbrushes due to a potential choking hazard from small parts if used beyond the recommended 3-month brush head life.
Maquet is recalling specific Magnus carbon-fibre operating table tops due to a potential issue with motor brakes for the longitudinal shift and tilt drives.
Church & Dwight is recalling Arm and Hammer Spinbrush Pro Clean Sonic Trays due to a potential small parts choking hazard if used beyond the recommended 3-month brush head life.
Church & Dwight is recalling Arm and Hammer Spinbrush Pro Clean Sonic Recharge units due to a potential small parts choking hazard when used beyond the recommended brush head life.
Church & Dwight is recalling Arm and Hammer Spinbrush toothbrushes due to a potential choking hazard from small parts if used beyond the recommended brush head life.
GE OEC Medical Systems is recalling OEC MiniView 6800 Mobile C-Arms due to a hard disk drive issue. The recall covers 82 units distributed worldwide.
Intuitive Surgical is recalling specific lots of da Vinci Instrument Arm Drapes because the sterile adaptor may have difficulty engaging an instrument.
ICU Medical is recalling specific lots of 94-inch IV administration sets because a molding defect may cause side ports to become occluded.
Intuitive Surgical is recalling specific lots of da Vinci Instrument Arm Drapes because the sterile adaptor may have difficulty engaging an instrument.