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
Boston Scientific is recalling ACCOLADE MRI EL DR pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Hologic, Inc. is correcting 12 Affirm Lateral Arm Upright Biopsy Accessories in the U.S. due to a component issue that could impact needle alignment during lateral biopsy procedures.
Fujifilm is recalling Aspire Cristalle mammography machines because the swivel arm may move down unintentionally.
Boston Scientific is recalling ESSENTIO DR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Boston Scientific is recalling VISIONIST CRT-P pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Boston Scientific is recalling ESSENTIO MRI SR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Boston Scientific is recalling PROPONENT EL DR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Owen Mumford USA is recalling Unifine Pentips pen needles because water exposure may have compromised sterility. Consumers should check for discoloration on the protective seal.
Philips is recalling one Ingenuity Core CT scanner because certain fasteners cannot be confirmed to be torqued to specification, posing a potential risk of harm if parts become loose during use.
Boston Scientific is recalling ALTRUA 2 DR pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Hamilton Medical is recalling 176 Intellicuff Standalone devices because the motor may cease to function during use, potentially affecting endotracheal tube cuff pressure.
Boston Scientific is recalling ESSENTIO MRI EL DR Pacemakers because reports indicate the Minute Ventilation sensor may intermittently over-sense signals.
Boston Scientific is recalling ESSENTIO MRI DR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Boston Scientific is recalling ESSENTIO SR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Phadia US Inc is recalling 70 Phadia 1000 Instruments nationwide because a malfunctioning Retry command may cause solution shortages and affect test results.
Boston Scientific is recalling ACCOLADE DR pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Medtronic is recalling KYPHON Express Directional Bone Filler Devices because the directional arrow may not align with the opening.
Boston Scientific is recalling ACCOLADE EL DR pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Boston Scientific is recalling ACCOLADE MRI DR Pacemakers because reports indicate the Minute Ventilation sensor may intermittently over-sense signals.
Boston Scientific is recalling PROPONENT DR Pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Philips is recalling 13 Brilliance iCT scanners because certain fasteners may not have been torqued to specification, posing a potential risk of harm if parts become loose during use.
Boston Scientific is recalling ACCOLADE SR pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Boston Scientific is recalling VALITUDE CRT-P pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Boston Scientific is recalling PROPONENT MRI Pacemakers because of reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Boston Scientific is recalling VALITUDE X4 CRT-P pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.