Home › Device types › FFF
Cover, Biopsy Forceps
FDA product code FFF · Class 1 · Gastroenterology, Urology
1
Registered devices
5
Adverse events
5
Recalls
1
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-12-18 | Wilson-Cook Medical Inc. | The product is being recalled because Captura Serrated Forceps with Spike (DBF-2.4SN-230SP-20-S) were mislabeled as Captura Serrated Large Forcep-No Spike (DBF- |
| 2018-12-18 | Wilson-Cook Medical Inc. | The product is being recalled because Captura Serrated Forceps with Spike (DBF-2.4SN-230SP-20-S) were mislabeled as Captura Serrated Large Forcep-No Spike (DBF- |
| 2007-08-28 | Boston Scientific Corporation | Device lacked manufacturing finishing process resulting in endoscope damage. |
| 2007-08-28 | Boston Scientific Corporation | Device lacked manufacturing finishing process resulting in endoscope damage. |
| 2007-08-28 | Boston Scientific Corporation | Device lacked manufacturing finishing process resulting in endoscope damage. |
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