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_DEVICE Z-2468-2025.
Pending LLM rewrite. Source: NHTSA 24V125000.
Pending LLM rewrite. Source: NHTSA 24V124000.
Pending LLM rewrite. Source: NHTSA 24V128000.
Pending LLM rewrite. Source: CPSC 25447.
Pending LLM rewrite. Source: CPSC 25450.
Pending LLM rewrite. Source: CPSC 25452.
Pending LLM rewrite. Source: CPSC 25451.
Pending LLM rewrite. Source: CPSC 25444.
Pending LLM rewrite. Source: CPSC 25445.
Pending LLM rewrite. Source: CPSC 25449.
Pending LLM rewrite. Source: FDA_DEVICE Z-2345-2025.
Pending LLM rewrite. Source: FDA_FOOD H-0518-2025.
Pending LLM rewrite. Source: FDA_FOOD H-0508-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2330-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2339-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2329-2025.
Pending LLM rewrite. Source: FDA_FOOD H-0515-2025.
Pending LLM rewrite. Source: FDA_FOOD H-0504-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2338-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2326-2025.
Pending LLM rewrite. Source: FDA_FOOD H-0519-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0592-2025.
Pending LLM rewrite. Source: FDA_FOOD H-0516-2025.
Pending LLM rewrite. Source: FDA_FOOD H-0513-2025.