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BOSS Instruments
BOSS INSTRUMENTS, LTD., INC. · Model 79-0330 · UDI-DI 00888515204591
GEJ
Prescription
5
510(k) clearances
9
Adverse events
4
Recalls
72
Facilities
Description
Wire Passer, Cannulated, 45mm dia, 7"
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-04-25 | Cook Inc. | reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products |
| 2017-04-25 | Cook Inc. | reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products |
| 2017-04-25 | Cook Inc. | reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products |
| 2006-10-12 | Conmed Corporation | The grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube. |
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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.