Class IIOngoingZ-1310-2025
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BH198R
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Aesculap IncPAMar 19, 2025
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–2 of 2 recalls
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Reports of various packaging issues that may result in a breach of the sterile barrier.