Medical DeviceMar 11, 2026
AESCULAP MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM recall — FDA Z-1485-2026
There is the potential for the length of the trocar shaft to be too long.
Class IIFDA: OngoingAesculap Inc
Recall history in this database
Classification mix: Class II: 14.
Medical DeviceNov 5, 2025
Aesculap SEALING UNIT F/10/12MM TROCARS W.REDUCER recall — FDA Z-0309-2026
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceNov 5, 2025
AESCULAP REDUCING CONVERTER 10/12MM TO 5MM recall — FDA Z-0312-2026
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceNov 5, 2025
Aesculap SEALING CAP FOR 10/12MM TROCARS recall — FDA Z-0310-2026
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceNov 5, 2025
AESCULAP SEALING UNIT FOR 10/12MM TROCARS recall — FDA Z-0311-2026
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceMar 19, 2025
Aesculap Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil recall — FDA Z-1312-2025
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceMar 19, 2025
Aesculap Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf recall — FDA Z-1308-2025
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceMar 19, 2025
Aesculap Numerous models of nonsterile hemostatic forceps: (1) REF BH100R, Carrel Artery recall — FDA Z-1309-2025
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceMar 19, 2025
Aesculap Numerous models of nonsterile hemostatic forceps: (1) REF FB458R, Glover ATR.CLAMP recall — FDA Z-1311-2025
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceMar 19, 2025
Aesculap Numerous models of nonsterile hemostatic forceps: (1) REF BH198R, Fuchsig Artery recall — FDA Z-1310-2025
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceJun 19, 2024
Aesculap Aeos Robotic Digital Microscope, Product Code: PV010 recall — FDA Z-2139-2024
Possibility of the robotic arm to drop more than 10cm from its original position after pressing the emergency stop button due to failure of the integrated safety mechanism.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceMar 13, 2024
Aesculap DISP.TROCAR W. DILATING PIN 10/110MM, Product Code EK224SU. For use in laparoscopic recall — FDA Z-1243-2024
The sterile blister packaging may be damaged, and sterility may be compromised.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceFeb 7, 2024
Aesculap MB215R - MILLS DUROGRIP TC Micro Needle Holder, straight, 8:, (203 mm), "TC MILLS recall — FDA Z-0867-2024
Needle Holder MB215R was inadvertently distributed as MB362R. Similarly, MB362R was distributed as MB215R during the affected distribution date range. The issue may lead to a short delay in…
Class IIFDA: OngoingAesculap Inc.
Medical DeviceFeb 7, 2024
Aesculap MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC recall — FDA Z-0866-2024
Needle Holder MB215R was inadvertently distributed as MB362R. Similarly, MB362R was distributed as MB215R during the affected distribution date range. The issue may lead to a short delay in…
Class IIFDA: OngoingAesculap Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Aesculap Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.