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AESCULAP
Aesculap AG · Model LX171R · UDI-DI 04038653050086
HYA
Prescription
0
510(k) clearances
11
Adverse events (1 deaths)
1
Recalls
107
Facilities
Description
Wire Holding Forceps, 6 3/4", (170 mm), longitud. transversal grooves, non-sterile, reusable
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. |
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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.