Weck EFx Classic Fascial Closure System — Class II medical device recall Z-2538-2016
Terminated recall by Teleflex Medical, reported 2016-08-24, distributed nationwide. Incorrect expiration date was printed on the product label.
| Recall number | Z-2538-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2016-03-24 |
| Classified | 2016-08-15 |
| Reported by FDA | 2016-08-24 |
| Terminated | 2020-09-25 |
| Distributed | Nationwide (US) |
| Quantity | 45 |
| Reason classes | labeling |
| Lot numbers | ML-000342, ML-000343, ML-000344, ML-000345, ML-000347, ML-000348, ML-000349 |
Product
Weck EFx Classic Fascial Closure System, Rx Only, Sterile, The product is intended to facilitate placement and withdrawal of suture loops to repair port side defects following laparoscopic surgery
Reason for recall
Incorrect expiration date was printed on the product label.
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-2538-2016. 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.