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SURGISTAR
SURGISTAR, INC. · Model 882859 · UDI-DI 00878799001030
10
510(k) clearances
82
Adverse events
9
Recalls
226
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-05-07 | MicroAire Surgical Instruments, LLC | Potential that the blade can unintentionally cut tissue prior to the user deploying the blade. |
| 2020-05-18 | Carefusion 2200 Inc | Becton Dickinson and Company, is conducting a voluntary recall on the V. MuellerTM 3H Knife Handles catalog number listed in the table above. BD has been informed by our supplier t |
| 2018-05-14 | Beaver Visitec | Blades are loose in handles and may fall out due to non cured epoxy |
| 2017-11-03 | Beaver-Visitec International Inc. | The protective shield was retracted, and the blade was exposed. |
| 2017-11-03 | Beaver-Visitec International Inc. | The protective shield was retracted, and the blade was exposed. |
| 2017-11-03 | Beaver-Visitec International Inc. | The protective shield was retracted, and the blade was exposed. |
| 2017-11-03 | Beaver-Visitec International Inc. | The protective shield was retracted, and the blade was exposed. |
| 2017-11-03 | Beaver-Visitec International Inc. | The protective shield was retracted, and the blade was exposed. |
| 2013-05-03 | Surgical Instrument Service And Savings, Inc. | The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch. |
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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.