Aesculap recalls
7 official recalls and safety alerts involving Aesculap since 2024-02, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Aesculap or the relevant agency.
- 2026-03-11
USAesculap Inc recalls Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product…
There is the potential for the length of the trocar shaft to be too long.
FDA · DeviceAesculap IncUS Nationwide distribution in the states of AZ, AR, CA, CO, FL, GA, HI, IA,…Official notice →- 2025-11-05
- US
Aesculap Inc recalls Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number: EK083P Software Version: N/A Product…
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
FDA · DeviceAesculap IncWorldwide - US Nationwide distribution in the states of AR, AZ, CA, CT, MD,…Official notice → - 2025-10-08
- US
Aesculap AG recalls AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R.
Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long" and the ELAN 4 FIXED DURAGUARD LONG was labeled as "Standard."
FDA · DeviceAesculap AGUS distribution to Missouri. OUS International distribution to Norway,…Official notice → - 2025-03-19
- US
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R, Negus Tonsil Forceps…
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
FDA · DeviceAesculap IncDistribution was made nationwide and to PR. There was also government/military…Official notice → - 2024-06-19
- US
Aesculap Inc recalls Aeos Robotic Digital Microscope, Product Code: PV010
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.
FDA · DeviceAesculap IncUS Nationwide distribution in the states of AR, FL, IL, IN, KY, MI, NC, NE,…Official notice → - 2024-03-13
- US
Aesculap Inc recalls DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.
The sterile blister packaging may be damaged, and sterility may be compromised.
FDA · DeviceAesculap IncWorldwide - US Nationwide distribution in the states of KS, NJ and NY. The…Official notice → - 2024-02-07
- US
Aesculap Inc recalls MB215R - MILLS DUROGRIP TC Micro Needle Holder, straight, 8:, (203 mm), "TC MILLS NDLE HOLDRRND HNDLSTR203MM"
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 procedure.
FDA · DeviceAesculap IncUS Nationwide distribution in the states of CA, CO, FL, ID, KY, MD, MO, MT,…Official notice →