[pending] EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180
Pending LLM rewrite. Source: FDA_DEVICE Z-0046-2026.
- Product
- EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180
- Category
- Medical Device
- Distribution
- Distributed nationwide
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_DEVICE Z-0046-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0093-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0185-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0174-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0198-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0048-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0165-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0148-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0193-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0062-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0109-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0087-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0050-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0104-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0173-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0059-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0031-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0053-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0205-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0169-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0202-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0056-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0085-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0105-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0141-2026.