[pending] DxC 700 AU, REF: B86444, B86446
Pending LLM rewrite. Source: FDA_DEVICE Z-1552-2026.
- Product
- DxC 700 AU, REF: B86444, B86446
- Category
- Medical Device
- Distribution
- Distributed nationwide
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-1552-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1500-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1508-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1529-2026.
CNC Noodle Corporation is recalling ZHONG HUA CHAO MIAN fresh noodles due to undeclared wheat and Yellow #6 food coloring on the label. Consumers with wheat allergies or sensitivities to the colorant may be at risk.
Pending LLM rewrite. Source: FDA_DEVICE Z-1543-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1524-2026.
House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream (3 gallon tubs) is being recalled because it contains undeclared egg, a common allergen. The recall affects 4,880 tubs distributed in Illinois.
Polski Ogrod Sp. z o.o. is recalling Hortex Mieszanka 9 Spring vegetable mix due to potential glass contamination. The affected product was distributed in Illinois.
Pending LLM rewrite. Source: FDA_DEVICE Z-1535-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1558-2026.
Pending LLM rewrite. Source: CPSC 26324.
Pending LLM rewrite. Source: CPSC 26323.
Pending LLM rewrite. Source: CPSC 26321.
Pending LLM rewrite. Source: CPSC 26320.
Pending LLM rewrite. Source: CPSC 26319.
Pending LLM rewrite. Source: FDA_DRUG D-0365-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1488-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1469-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0375-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0384-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0373-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0371-2026.
Pending LLM rewrite. Source: NHTSA 24V898000.
Pending LLM rewrite. Source: FDA_DEVICE Z-1478-2026.