Class II — Aesculap Inc
| Recalling firm | AESCULAP, INC. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The sterile blister packaging may be damaged, and sterility may be compromised. |
| Product | DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures. |
| Quantity | 18 pieces |
| Distribution | Worldwide - US Nationwide distribution in the states of KS, NJ and NY. The country of Canada. |
| Initiated | 2024-01-09 |
| Classified | 2024-03-01 |
| Recall number | Z-1244-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Aesculap Inc (Z-1244-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93856/
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