DISP — Class II medical device recall Z-1243-2024
Ongoing recall by Aesculap Inc, reported 2024-03-13, distributed nationwide. The sterile blister packaging may be damaged, and sterility may be compromised.
| Recall number | Z-1243-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aesculap Inc, Center Valley, PA, United States |
| Recall initiated | 2024-01-09 |
| Classified | 2024-03-01 |
| Reported by FDA | 2024-03-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 12 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 04046963620424 |
| Lot numbers | 52567841, 52625350, 52658689 |
Product
DISP.TROCAR W. DILATING PIN 10/110MM, Product Code EK224SU. For use in laparoscopic procedures.
Reason for recall
The sterile blister packaging may be damaged, and sterility may be compromised.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1243-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.