WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips — Class II medical device recall Z-0826-2015
Terminated recall by Teleflex Medical, reported 2014-12-24, distributed nationwide. The manufacturing dates and expiration dates were transposed on the Tyvek label.
| Recall number | Z-0826-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Durham, NC, United States |
| Recall initiated | 2014-12-03 |
| Classified | 2014-12-17 |
| Reported by FDA | 2014-12-24 |
| Terminated | 2017-11-24 |
| Distributed | Nationwide (US) |
| Quantity | 3,180 units |
| Reason classes | labeling |
| Lot numbers | 01B1400034 |
Product
WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are intended for use in procedures involving vessels or anatomic structures for which the surgeon determines ligating clips are the best choice.
Reason for recall
The manufacturing dates and expiration dates were transposed on the Tyvek 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-0826-2015. 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.