ConMed Anchor Tissue Retrieval System — Class II medical device recall Z-1308-2019
Terminated recall by Conmed Corporation, reported 2019-05-15, distributed nationwide. Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
| Recall number | Z-1308-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Conmed Corporation, Utica, NY, United States |
| Recall initiated | 2019-03-21 |
| Classified | 2019-05-09 |
| Reported by FDA | 2019-05-15 |
| Terminated | 2023-01-17 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, CA, DK, ES, GB, IE, JP, NL, OM, PL, QA, RO, SE, SG |
| Quantity | 1,310 |
| Reason classes | sterility, packaging |
| Lot numbers | 19A8T, 20180426X, 201901244, 201901254, 201901284, 201901294, 201902159, 20190215X, 68A8T, TRS-ROBO-8 |
| Model numbers | 201901244, 201901254, 201901284, 201901294, TRS-ROBO-8 |
Product
ConMed Anchor Tissue Retrieval System, 8 MM, 125 ML (5/BX) Catalog Number:TRS-ROBO-8 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during laparoscopic surgery.
Reason for recall
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
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-1308-2019. 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.