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
Biomet is recalling G7 Acetabular System Positioning Guide Rods because they may fracture during surgery, potentially causing retained fragments or surgical delays.
Philips is recalling Height Adjustable FlexTrak trolleys and Trolley Variable Height IRFs for Ingenia MR systems due to a risk of foot clamping.
Boston Scientific is recalling 968 IntellaTip MiFi XP Temperature Ablation Catheters because some units were not manufactured according to specification.
Nellcor Puritan Bennett Inc. is recalling Backlight Inverter Printed Circuit Boards for PB840 Ventilators due to a potential loss of the graphical user interface display.
Biomet, Inc. is recalling 102 EZPass Suture Passers because the nitinol wire may buckle and become kinked, making the instrument difficult to use.
RaySearch Laboratories is recalling RayStation software version 4.0.3.4 due to a bug that causes incorrect dose calculations for radiation therapy plans with variable CT slice spacing.
Boston Scientific is recalling 968 IntellaTip MiFi XP Temperature Ablation Catheters because some units were not manufactured according to specification.
Biomet is recalling G7 Acetabular System Positioning Guide Posts because the guide rod may fracture during surgery, potentially causing a delay in the procedure.
Elekta, Inc. is recalling Synergy XVI radiation therapy systems because they may incorrectly calculate the treatment table's target position.
Philips is recalling Ingenia HA FLEX TRAK Trolleys because the central column can clamp a patient's foot. The recall covers 420 units distributed worldwide.
Spacelabs Healthcare is voluntarily recalling Ventilator Flexport Interfaces because the bedside monitor may display minute volume values up to ten times the actual value.
ConMed Corporation is recalling Altrus Thermal Tissue Fusion Handpieces due to a risk of burns. The recall covers 12,653 units distributed worldwide.
GE Healthcare is recalling Compact Airway Modules because a loose screw may cause pump failure, leading to loss of respiratory gas monitoring.
Ebi, LLC is recalling 32 units of the Biomet Spine Cypher MIS Screw Inserter due to an increased rate of instrument tip failure.
Ability Dynamics is recalling 175 RUSH81 prosthetic feet because existing bolts may be bottomed out in threaded holes, which could lead to bolt failure.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products FS Calibrator 1 because calibrator values were assigned using a reference method that was not fully validated.
Kerr Corporation is recalling one lot of Tytin Regular Set dental restorative material because it may set faster than specified in the Directions for Use.
Elekta, Inc. is recalling 224 iGUIDE Systems because a software bug prevents the system from logging off. The recall covers units distributed worldwide.
Elekta, Inc. is recalling MOSAIQ oncology software versions 1.40 through 2.50 because scrolling actions can unintentionally change direction selections.
Roche Diagnostics is recalling cobas 6000 analyzer filters that may cause discrepant results and system alarms.
Roche Diagnostics is recalling cobas 8000 analyzer filters that may cause discrepant results, alarms, or foam under certain conditions.
Boston Scientific is recalling 968 IntellaTip MiFi XP Temperature Ablation Catheters because some units were not manufactured according to specification.
Nipro Medical Corporation is recalling NIPRO Safe Touch Safety Scalp Vein Sets because a crack in the connector could cause fluid leakage.
Children's Medical Ventures is recalling 112 infant apnea monitors due to a battery wire harness defect that renders the devices inoperable.
Biomet is recalling 100 units of EZPass Suture Retriever instruments because the nitinol wire may buckle and become kinked, making the device difficult to use.