Aesculap Inc recalls

10 recalls on record · latest: January 15, 2026

Official U.S. recall history for Aesculap Inc, compiled from official government records.

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Aesculap Inc recalls Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Versio…

January 15, 2026 · Medical device recalls Moderate risk There is the potential for the length of the trocar shaft to be too long.

Aesculap Inc recalls Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Model/Catalog Number: EK086P Software Version: N/A…

September 24, 2025 · Medical device recalls Moderate risk It was determined there is the potential of silicone fragments detaching from t…

Aesculap Inc recalls Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Model/Catalog Number: EK085P Software Version: N/A P…

September 24, 2025 · Medical device recalls Moderate risk It was determined there is the potential of silicone fragments detaching from t…

Aesculap Inc recalls Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P Software Version: N/A…

September 24, 2025 · Medical device recalls Moderate risk It was determined there is the potential of silicone fragments detaching from t…

Aesculap Inc recalls Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number: EK083P Software Versi…

September 24, 2025 · Medical device recalls Moderate risk It was determined there is the potential of silicone fragments detaching from t…

Numerous models of nonsterile hemostatic forceps: REF BH198R recalled over sterility concerns

January 31, 2025 · Medical device recalls Moderate risk The forceps have been used in ways not covered by the design resulting in break…

Numerous models of nonsterile hemostatic forceps: REF FB458R recalled over sterility concerns

January 31, 2025 · Medical device recalls Moderate risk The forceps have been used in ways not covered by the design resulting in break…

Numerous models of nonsterile hemostatic forceps: REF BH100R recalled over sterility concerns

January 31, 2025 · Medical device recalls Moderate risk The forceps have been used in ways not covered by the design resulting in break…

Numerous models of nonsterile hemostatic forceps: REF BJ500R recalled over sterility concerns

January 31, 2025 · Medical device recalls Moderate risk The forceps have been used in ways not covered by the design resulting in break…

Numerous models of nonsterile hemostatic forceps: REF BH951R recalled over sterility concerns

January 31, 2025 · Medical device recalls Moderate risk The forceps have been used in ways not covered by the design resulting in break…