Home › MARINA MEDICAL INSTRUMENTS, INC. › Marina Medical
Marina Medical
MARINA MEDICAL INSTRUMENTS, INC. · Model 337-240 · UDI-DI 00840306808142
5
510(k) clearances
9
Adverse events
4
Recalls
72
Facilities
Description
Miyazaki Tack Driver
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. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.