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Disposable Non-electric Biopsy Forceps

Jiangsu Vedkang Medical Science and Technology Co.,Ltd. · Model VDK-FB-23-230-W-P1-A1 · UDI-DI 06970057574486

FCL Prescription

510(k) clearances

2,705

Adverse events (17 deaths)

Recalls

190

Facilities

Recalls

Date	Firm	Reason
2026-06-30	Boston Scientific Corporation	Potential for breach in sterile barrier of device packaging.
2026-06-30	Boston Scientific Corporation	Potential for breach in sterile barrier of device packaging.
2026-06-30	Boston Scientific Corporation	Potential for breach in sterile barrier of device packaging.
2023-03-24	Richard Wolf GmbH	Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be open
2023-03-24	Richard Wolf GmbH	Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be open
2023-03-24	Richard Wolf GmbH	Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be open
2023-03-24	Richard Wolf GmbH	Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be open
2016-04-15	Cook Inc.	Increase in reports of polymer degradation of the catheter tip, resulting in tip fracture and/or separation. degradation could include loss of device function, separation of a devi
2010-05-06	Boston Scientific Corporation	Clevis may detach from the coil preventing the device to open and/or close. Delays in the procedure may result.
2010-05-06	Boston Scientific Corporation	Clevis may detach from the coil preventing the device to open and/or close. Delays in the procedure may result.

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Data 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.