Home › STERIS CORPORATION › V. Mueller
V. Mueller
STERIS CORPORATION · Model BE2472 · UDI-DI 10885403015182
KAE
Prescription
10
510(k) clearances
89
Adverse events
1
Recalls
226
Facilities
Description
V. Mueller LARYNGEAL, BRONCHIAL GRASPING FORCEPS, GRASPING TIP 3 X 11MM SERRATED, PASS DIAMETER 4.5MM WORKING LENGTH 15-3/4 inches 40CM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
