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ACCULAN II
Aesculap AG · Model GB439R · UDI-DI 04038653237494
HXY
Prescription
7
510(k) clearances
44
Adverse events
1
Recalls
93
Facilities
Description
ACCULAN II K-WIRE CHUCK MIDDLE LEVER
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-05-27 | Musculoskeletal Transplant Foundation, Inc. | Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix Insertion Kits because they are labeled as having a 2.0mm diameter drill however it may contain a 2.4 mm |
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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.