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Cable-Ready®
Zimmer, Inc. · Model 2232-50-08 · UDI-DI 00889024039643
HXQ
Prescription
0
510(k) clearances
13
Adverse events
1
Recalls
52
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-09-26 | Biomet, Inc. | An investigation identified that high level friction may exist between the needle and Mamba suture passer instrument, causing the needle to break 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.