WECK — Class II medical device recall Z-0083-2018
Terminated recall by Teleflex Medical, reported 2017-11-15, distributed nationwide. The product has a non-conformity that may cause clips to mislead, jam or fall out of the applier.
| Recall number | Z-0083-2018 |
|---|---|
| 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 | 2017-10-05 |
| Classified | 2017-11-09 |
| Reported by FDA | 2017-11-15 |
| Terminated | 2023-01-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BE, CA, CN, JP, KR, SG, TH, TW |
| Quantity | 13,710 units |
| Lot numbers | 73A1700701, 73B1700183, 73B1700567, 73C1600069, 73C1600070, 73C1600071, 73C1700288, 73C1700289, 73C1700290, 73C1700292, 73C1700300, 73F1600036, 73F1600037, 73F1600038, 73F1600039, 73F1600040, 73F1600689, 73F1600690, 73F1600691, 73F1600692, 73F1600693, 73F1600694, 73G1600151, 73G1600431, 73G1600432, 73G1600716, 73G1600717, 73H1500014, 73H1500015, 73H1500016, 73H1600173, 73H1600174, 73H1600582, 73H1600583, 73H1600663, 73H1600664, 73H1600665, 73H1600666, 73H1600667, 73H1600668 and 24 more |
| Model numbers | AE05ML |
Product
WECK(R) from TELEFLEX Auto Endo5(R), Automatic Hem-o-lok(R) Clip Applier, REF AE05ML (IPN010797) Rx ONLY, STERILE EO
Reason for recall
The product has a non-conformity that may cause clips to mislead, jam or fall out of the applier.
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-0083-2018. 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.