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NA 829051Recalls & reported problems

Richard Wolf GmbH · FLEX. BIOPSY FORCEPS 5FR WL 550MM double action, TL 720 mm, non-dismantling, reusable · Class 1

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Mar 24, 2023Open, Classified

    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 opened or restrictions begin even with a slight bending of the endoscope.

    Z-1423-2023 · Root cause: Under Investigation by firm · FDA record ↗

Other FORCEPS, BIOPSY, NON-ELECTRIC devices

All FORCEPS, BIOPSY, NON-ELECTRIC devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.