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.
Minimum severity
Pending LLM rewrite. Source: FDA_FOOD H-0840-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0782-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0789-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0818-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0830-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0792-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0832-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0784-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0802-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0785-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0833-2026.
Tangent Endoscopy is recalling its Tangent Single Use Digital Catheter (models TNG4002-IND and TNG-4007-6pk) due to fractures observed at the distal shaft tip without complete detachment, posing a risk during endoscopic procedures.
The deaeration hose in Philips Azurion X-ray tube cooling units may degrade over time and leak oil, affecting cooling performance and automatically triggering low-dose fluoroscopy mode.
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94915), a cardiopulmonary bypass vascular catheter, due to potential sterile barrier breach.
Pending LLM rewrite. Source: FDA_FOOD H-0842-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0786-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0810-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0846-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0819-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0821-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0796-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0841-2026.
Lupin Pharmaceuticals is recalling Liraglutide Injection due to the presence of white thread-like structures (particulate matter) found in cartridges. The recall affects 217,621 pen injectors distributed nationwide.
Becton, Dickinson and Company is recalling Swan-Ganz Jr Catheters (models SGPT54, SGPT64P, SGPT755P) because the blue proximal injectate lumen hub may leak or break due to manufacturing changes, risking infection, medication loss, and blood loss.
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula (Model 94913), a cardiopulmonary bypass vascular catheter, due to a potential sterile barrier breach.