Data Foundry

Medical device recalls 2019

ConMed Anchor Tissue Retrieval System 15 MM — Class II medical device recall Z-1305-2019

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 numberZ-1305-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmConmed Corporation, Utica, NY, United States
Recall initiated2019-03-21
Classified2019-05-09
Reported by FDA2019-05-15
Terminated2023-01-17
DistributedNationwide (US)
Countries outside the USAT, CA, DK, ES, GB, IE, JP, NL, OM, PL, QA, RO, SE, SG
Quantity11,835
Reason classessterility, packaging
Lot numbers19A8T, 20180426X, 201808025, 201809205, 201809215, 201901154, 201901164, 201901174, 201901184, 201901214, 201901224, 201902159, 20190215X, 68A8T, TRS175SB2
Model numbers201808025, 201809205, 201809215, 201901154, 201901164, 201901174, 201901184, 201901214, 201901224, TRS175SB2

Product

ConMed Anchor Tissue Retrieval System 15 MM, 1550 ML (3/BX) Catalog Number: TRS175SB2 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-1305-2019. 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.