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
Ortho Development Corporation is recalling 29 tibial tray components due to a manufacturing defect that may cause assembly resistance.
Nobel Biocare is recalling 238 Universal Base CC RP 1.5 mm abutments because they may contain incorrect screws that could loosen.
Nobel Biocare is recalling 478 Temporary Snap Abutments because packages may contain incorrect screws that could loosen, requiring retightening.
Nobel Biocare is recalling 239 units of Temporary Abutment Engaging CC RP components because packages may contain incorrect screws that could loosen.
ICU Medical is recalling 123 units of the Cogent Hemodynamic Monitoring System because a software issue prevents the system from storing patient IDs and information.
Trilliant Surgical, LLC is recalling 3.5mm Aresenal Screw Drill Bits due to a labeling error where the lot number is incorrectly marked, potentially impacting device traceability.
TeDan Surgical Innovations LLC is recalling Fukushima suction tubes because incorrect raw material was used in production. The affected units were distributed in New Jersey.
Ivoclar Vivadent AG is recalling 639 units of IPS e.max ZirCAD ceramic blocks because they crack during the sintering process.
Inpeco S.A. is recalling 65 FlexLab Centrifuge Modules because a tube loading algorithm defect may cause unbalanced loads that could damage the equipment.
Nobel Biocare is recalling 228 dental implants because the packaging label incorrectly lists the length as 7mm instead of the actual 10mm.
Gentell, Inc. is recalling Gentell Honey Hydrogel because the product was not properly registered with the FDA, as discovered during an audit.
Nobel Biocare is recalling 236 units of temporary dental implant abutments because packages may contain an incorrect screw that could loosen.
Inpeco S.A. is recalling 313 Siemens Aptio Automation Centrifuge Modules because a tube loading algorithm may cause unbalanced loads that could damage the centrifuge.
Philips is recalling two Brilliance iCT SP CT scanners because a cooling unit bolt was not tightened to specification.
Epimed International is recalling 701 units of R-F Injector Cannulas due to incorrect expiration dates on the packaging. The devices were distributed worldwide and across multiple US states.
Nobel Biocare is recalling 227 Esthetic Abutment CC RP 1.5 mm units because they may contain incorrect screws that could loosen.
Northgate Technologies is recalling 9 FR AUTOLITH probes because a lot failed biocompatibility testing. The recall covers 298 boxes distributed nationwide.
R82 A/S is recalling 2,230 chest supports for the R82 Mustang and Rabbit Up because a plastic plug can come loose without tools.
Wright Medical Technology Inc is recalling 22 units of Inbone Tibial Trays because one lot is missing the required plasma coating.
Abbott Laboratories is recalling 65 kits of ARCHITECT C Peptide Calibrators distributed in Mexico due to an error in the renewal documentation process for the local license.
Abbott Laboratories is recalling 65 kits of ARCHITECT C Peptide Reagents in Mexico due to an error in the license renewal documentation process.
Gentell, Inc. is recalling 22,439 units of Gentell Honey Hydrogel 4"x4" Saturated Gauze because the product was not properly registered with the FDA.
Gentell, Inc. is recalling 4,348 units of Gentell Honey Hydrogel Saturated Gauze because the product was not properly registered with the FDA.
Gentell, Inc. is recalling 85,586 units of Gentell Honey Hydrogel 2"x2" Saturated Gauze because the product was not properly registered with the FDA.
Epimed International is recalling 1,374 units of RF Injector Cannulas due to incorrect expiration dates on the packaging.