Class IIOngoingZ-1309-2025
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BH100R
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.
Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.