Home › CAREFUSION 2200, INC › V. Mueller
V. Mueller
CAREFUSION 2200, INC · Model BE752 · UDI-DI 10885403014840
KAE
Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
225
Facilities
Description
FRAENKEL LARYNGEAL FORCEPS LATERAL BITING ALLIGATOR PATTERN WORKING LENGTH 8" (20.3CM)
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.