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
Medtronic Navigation is voluntarily recalling 111 AxIEM Touch N Go Pointer Probes because they may compromise navigation accuracy during patient registration.
Symmetry Surgical is recalling ULTRA Steam containers because deteriorated or missing base trim sealant may allow contaminants to enter after sterilization.
Beckman Coulter is recalling the DxH 600 Cellular Analysis System because it may fail to detect blasts in some blood samples.
Amendia, Inc. is recalling six Ceres-C Standalone Cervical Interbody devices because they are missing a tantalum market pin.
Siemens is recalling Artis Q angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.
ICU Medical is recalling Tego Connectors due to a potential risk of leaking. The devices are used as accessories for vascular access in hemodialysis.
Stryker is recalling reprocessed ablation catheter cables because a breach in sterile packaging may have resulted in non-sterile product.
Philips is recalling 41 Clinix RF Plus X-ray systems because liquid penetration can cause an unintentional tilt of the diagnostic table.
Symmetry Surgical is recalling 38 ULTRA Gravity sterilizer containers because deteriorated or missing base trim sealant could allow contaminants to enter the container.
In2Bones is recalling 40 units of NEOVIEW locking screws due to dimensional non-conformity of the thread on the screw head. The recall covers units distributed in the US, France, and Switzerland.
Beckman Coulter is recalling the UniCel DxH 800 Cellular Analysis System because it may fail to detect blasts in some blood samples.
Varian Medical Systems is recalling 42 Eclipse Treatment Planning System devices due to a software defect that prevents contours from saving consistently.
J&J Solutions, Inc. DBA Corvida Medical is recalling 5,520 Halo Closed System Transfer Devices because the needle does not retract. The devices were distributed in Maryland, Texas, and Wisconsin.
Health Robotics S.R.L. is recalling 121 i.v. Station and i.v. Station ONCO systems because a motor error caused misalignment and mislabeling of IV bags.
Natus Manufacturing Limited is recalling 31 Warmette Blanket and Dual Cabinets because a fuse may blow, causing power loss and potential melting of the fuse cover.
Zimmer Biomet is removing a specific lot of Oxford Fixed Lateral Bearings because packages labeled as 'Right' contained 'Left' bearings.
Advanced Sterilization Products is recalling 107 EVOTECH Endoscope Cleaner and Reprocessor Systems because a hose may come loose and cause a leak.
Merge Healthcare is recalling Merge Eye Station software versions 11.6.0 and prior due to a risk of accidental patient record deletion.
In2Bones is recalling 26 units of NEOVIEW Screws Set due to dimensional non-conformity of the thread on the screw head.
In2Bones is recalling 19 locking screws from the NEOVIEW Plating System due to dimensional non-conformity of the thread on the screw head.
Siemens Medical Solutions is recalling Biograph mCT Flow 40-4R scanners because laser cover windows may fall off.
Straumann Manufacturing is recalling 165 dental implant drills because they cannot be inserted into handpieces due to tolerance specification failures.
Siemens is recalling IMMULITE 2000 Intact PTH assay kits because they may show a negative bias of up to -39% at low concentrations.
ConforMIS is recalling iTotal PS Knee Replacement Kits because the iView software displayed femoral cut measurements in the wrong unit.
GE Healthcare is recalling OEC 9900 Elite and other mobile fluoroscopy systems because the workstation power cable assembly can fail intermittently.