Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1308-2025 — Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf Hysterectomy Forceps STR 210MM; (2) REF BJ501R, Phaneuf Hysterectomy Forceps ANG 205MM; (3) REF BJ511R, Holzbach Hyst Forceps CVD245MM; (4) REF BJ520R, Heaney Hyst Forceps Grooved 205MM; (5) REF BJ521R, Heaney Hyst Forc

U.S. FDA — Device Enforcement · United States · 2025-01-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1308-2025
Date of alert
2025-01-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Aesculap Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04038653139378
Reported risk: The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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