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
Zydus Pharmaceuticals is recalling erythromycin 500 mg tablets nationwide due to the presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit, resulting from manufacturing deviations.
Pending LLM rewrite. Source: FDA_FOOD H-0845-2026.
Medtronic is recalling certain lots of DLP Retrograde Cannula (Model 94913L), a cardiopulmonary bypass catheter, due to potential sterile barrier breaches. The affected device was distributed worldwide.
Pending LLM rewrite. Source: FDA_FOOD H-0806-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0824-2026.
Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94115T) cardiopulmonary bypass vascular catheters due to potential sterile barrier breach. The affected product has been distributed worldwide.
Pending LLM rewrite. Source: FDA_FOOD H-0834-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0823-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0790-2026.
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.
Pending LLM rewrite. Source: FDA_FOOD H-0838-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0833-2026.
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-0802-2026.
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula Model 94665 due to potential sterile barrier breach. The product is used in cardiopulmonary bypass procedures worldwide.
Pending LLM rewrite. Source: FDA_FOOD H-0816-2026.
ICU Medical is recalling Oncology Kits with extension sets due to potential leaks that could interrupt chemotherapy infusion and expose hazardous substances to patients, caregivers, and pharmacy technicians.
Pending LLM rewrite. Source: FDA_FOOD H-0795-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0799-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0811-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0815-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0820-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0836-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0804-2026.