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AESCULAP
Aesculap AG · Model LX149R · UDI-DI 04038653174850
HXZ
Prescription
1
510(k) clearances
513
Adverse events
1
Recalls
247
Facilities
Description
Wire Cutting Forceps, f.wire remov:after sternum sut, 6 3/4", (170 mm), slender pattern, special hardened cutting edges, soft wire up to Ø 0.9 mm, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-11-20 | Zimmer Biomet, Inc. | Device has the potential for fracture during use. |
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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.