Aesculap Inc DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures. Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.
Brand
Aesculap Inc
Lot Codes / Batch Numbers
Product Code: EK230SU, UDI/DI: 04046963620455, Batch Numbers (Expiration Date): 52481826 (02/29/2024), 52644661 (02/28/2026)
Products Sold
Product Code: EK230SU; UDI/DI: 04046963620455; Batch Numbers (Expiration Date): 52481826 (02/29/2024), 52644661 (02/28/2026);
Aesculap Inc is recalling DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures. due to The sterile blister packaging may be damaged, and sterility may be compromised.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The sterile blister packaging may be damaged, and sterility may be compromised.
Recommended Action
Per FDA guidance
URGENT MEDICAL DEVICE RECALL NOTIFICATION letters dated January 5, 2024 were sent to customers. Customers were instructed to cease use and quarantine all product subject to recall. Once Aesculap Customer Support receives the customer's acknowledgement form, they will contact the customer to arrange for credit and to have the current inventory returned.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026