Home › Aesculap AG › AESCULAP
AESCULAP
Aesculap AG · Model LX157R · UDI-DI 04038653050048
HXZ
Prescription
1
510(k) clearances
514
Adverse events
1
Recalls
247
Facilities
Description
HARVEY TC Wire Cutting Forceps, 9 1/4", (235 mm), special hardened cutting edges, hard wire up to Ø 2.2 mm, soft wire up to Ø 3.0 mm, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-11-20 | Zimmer Biomet, Inc. | Device has the potential for fracture during use. |
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.