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
Elekta is recalling 279 Monaco RTP Systems because they may calculate Enhanced Dynamic Wedge or Virtual Wedge values incorrectly.
Medline is recalling 12,024 tubes of E-Z Lubricating Jelly because they were not sterilized due to a shipping error.
Smith & Nephew is recalling Reflection Dead Blow Mallets because cracks in the weld allowed lead beads to escape into surgical wounds.
Stryker Howmedica Osteonics Corp. is recalling 131 units of the Reunion TSA Peg Alignment Sound because the instrument broke during surgery.
Alcon Research, Ltd. is recalling 1,130 Monarch III (1) "C" Cartridges because the intraocular lens could become lodged within the device.
Stryker Sustainability Solutions is recalling reprocessed electrophysiology catheter cables because a breach in sterile packaging may have occurred, potentially rendering the product non-sterile.
Elekta, Inc. is recalling Oncentra External Beam and Brachy software because a cross profile for a Varian 60-degree wedge shows 'horns.' The recall covers 433 units distributed worldwide.
Medtronic is recalling 21,111 MRI-conditional cardiac resynchronization therapy devices because the AdaptivCRT feature may appear enabled when it is not active.
C.R. Bard is recalling specific medical device trays and stabilization devices because they contained latex catheters instead of silicone catheters.
Symmetry Surgical is recalling 149 ULTRA Sterrad containers because deteriorated or missing base trim sealant may allow contaminants to enter the container after sterilization.
Philips is recalling 35 IQon Spectral CT systems due to software issues causing rescans, incorrect scan locations, or misrepresentation of image results.
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.