Home › CAREFUSION 2200, INC › V. Mueller
V. Mueller
CAREFUSION 2200, INC · Model OS3038 · UDI-DI 10885403102875
HYA
Prescription
0
510(k) clearances
11
Adverse events (1 deaths)
1
Recalls
108
Facilities
Description
V. Mueller VITAL ADVANCED 6MM JAW 7" EXTRACTION
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-06-17 | Biomet, Inc. | Medium Bone Plate Forceps was assembled with the incorrect grip arm tip. Potential that the surgeon will be unable to provisionally clamp the plate to the patient's bone. |
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.