Weck — Class II medical device recall Z-0770-2014
Terminated recall by Teleflex Medical, reported 2014-01-22, distributed nationwide. Sterility cannot be guaranteed.
| Recall number | Z-0770-2014 |
|---|---|
| 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 | 2013-12-19 |
| Classified | 2014-01-14 |
| Reported by FDA | 2014-01-22 |
| Terminated | 2016-05-20 |
| Distributed | Nationwide (US) |
| Quantity | 17,450 units |
| Reason classes | sterility |
| Lot numbers | 01A1100320, 01C1000012, 01C1000385, 01E1000392, 01M1000201 |
| Model numbers | 809600 |
Product
Weck, Electrosurgical Coagulation Suction Tube 6 (15.2cm), 11 French, with Stylet, Teleflex Medical, Research Triangle, NC 2770. Intended to remove tissue and control bleeding by use of high-frequency electrical current.
Reason for recall
Sterility cannot be guaranteed.
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-0770-2014. 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.