Every recall we track for Aesculap Inc — 18 in all — plus the complaints and injury reports the public filed about them.
Aesculap recalls MINOP Trocar 150mm 4-Wking Channel 6.0mm (model FF399R) due to potential for trocar shaft length being too long. Affected users should check serial numbers listed.
Aesculap recalls SEALING UNIT FOR 10/12MM TROCARS (model EK086P) due to potential silicone fragments detaching from the yellow sealing component. Affected units sold with specific lot numbers.
Aesculap recalls SEALING CAP FOR 10/12MM TROCARS (model EK085P) due to potential silicone fragments detaching. Affected units include specific production lots. Consumers should contact Aesculap for details.
Aesculap recalls reducing converters (model EK087P) due to potential silicone fragments detaching from the yellow sealing component. Affected units sold between 2020-2023; contact for return.
Aesculap recalls SEALING UNIT F/10/12MM TROCARS with model EK083P due to potential silicone fragments detaching from the sealing component. Affected units may cause injury if fragments enter the body during surgery.
Aesculap recalls 83 models of nonsterile hemostatic forceps due to breakage when used in ways not covered by design. Check product codes or GTINs for affected items.
Aesculap recalls 13 models of nonsterile hemostatic forceps due to breakage when used outside design specifications. Affected units include specific reference codes and GTINs.
Aesculap recalls 119 models of nonsterile hemostatic forceps due to breakage during use, which could lead to complications in medical procedures.
Aesculap recalls 18 models of nonsterile hemostatic forceps due to risk of clamp breakage during use. Affected models include REF BJ500R to REF MD592 with specific GTIN numbers.
Aesculap recalls several nonsterile hemostatic forceps models due to potential clamp breakage during use. Affected models include Negus and Schnidt Tonsil Forceps with specific reference numbers.
Aesculap recalls Aeos Robotic Digital Microscope (PV010) due to risk of robotic arm dropping more than 10cm after emergency stop. Affected units have specific serial numbers.
Aesculap recalls Disp.Hasson Trocar 12/110mm (Product Code EK240SU) due to potential sterility compromise from damaged blister packaging. Affected units sold with specific batch numbers and expiration dates.
Aesculap recalls laparoscopic trocars with possible sterility compromise due to damaged blister packaging. Affected units include specific product codes and batch numbers. Consumers should check packaging details to determine eligibility.
Aesculap recalls laparoscopic trocar pins with possible sterility compromise due to damaged packaging. Affected units have product code EK236SU and batch numbers ending 12/08/2023. Consumers should check packaging for damage before use.
Aesculap recalls laparoscopic trocar pins with possible sterility compromise due to damaged blister packaging. Affected units include Product Code EK234SU with batch 52573073 expiring 12/08/2023.
Aesculap recalls trocars with potential packaging damage that could compromise sterility during laparoscopic surgery. Affected units include specific product codes and batch numbers with expiration dates.
Aesculap recalls MB362R micro needle holders distributed between Nov 2022 and Oct 2023 due to potential short procedure delays. Affected items have UDI-DI 4046955075546.
Aesculap recalls MB215R micro needle holders distributed as MB362R between Nov 2022 and Oct 2023 due to potential procedure delays.
