Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Pending LLM rewrite. Source: FDA_FOOD H-0811-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0827-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0789-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0842-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0797-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0793-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0788-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0822-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0817-2026.
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-0844-2026.
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.
Philips Azurion X-ray imaging systems may experience impaired table movement due to mechanical wear in the Float Tabletop control. The control module defect could affect longitudinal and transverse table positioning during medical procedures.
Pending LLM rewrite. Source: FDA_FOOD H-0848-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0843-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0832-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0801-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0799-2026.
Becton, Dickinson and Company is recalling Swan-Ganz Pacing Catheter Model D200F7 due to a manufacturing defect that may cause the proximal injectate lumen hub to leak or break, potentially leading to infection, medication loss, or blood loss.
Pending LLM rewrite. Source: FDA_FOOD H-0834-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0838-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0802-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0840-2026.
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.
Pending LLM rewrite. Source: FDA_FOOD H-0787-2026.