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Rumex
RUMEX INTERNATIONAL CORP. · Model 12-211-23H · UDI-DI 00840159906910
10
510(k) clearances
385
Adverse events
2
Recalls
265
Facilities
Description
Straight Vitreoretinal Scissors, Attached To A Universal Handle, with a Flushing System, 23 Ga
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
| 2024-09-17 | MicroSurgical Technology Inc | Due to pin coming off of handles. |
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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.