RecallRadar

FDA Device recall Z-1307-2019

ConMed Anchor Tissue Retrieval System, VATS, 15 MM, 1550 ML (3/BX) Catalog Number: TRS-VATS-15 The Anchor Tissue Retrieval System" by CONME…

On 2019-05-15 the FDA classified a Class II recall of ConMed Anchor Tissue Retrieval System, VATS, 15 MM, 1550 ML (3/BX) Catalog Number: TRS-VATS-15 The Anchor Tissue Retrieval System" by CONME… by Conmed, citing voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1307-2019
ClassificationClass II
Statusterminated
Initiated2019-03-21
Published2019-05-15
Last updated2026-09-13 11:55 UTC
CompanyConmed
DistributionUS

Product

ConMed Anchor Tissue Retrieval System, VATS, 15 MM, 1550 ML (3/BX) Catalog Number: TRS-VATS-15 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

Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product

Identifiers

code_info
Lot codes for product manufactured to and including the dates listed below, with the exclusions noted below for each ca…Lot codes for product manufactured to and including the dates listed below, with the exclusions noted below for each catalog number: Beginning Manufacture Date: April 26, 2018 Beginning Lot Code: 20180426X Ending Manufacture Date: February 15, 2019 Ending Lot Code: 20190215X Excluded Anchor Tissue Retrieval System" Lot Codes - 1. All alpha/numeric lot codes (e.g. lots 68A8T or 19A8T) 2. All numeric lot codes ending with the number 9 (e.g. Lot code 201902159) 3. All excluded numeric lot codes listed in the tables below for each specific catalog number: Excluded Lot Code for Cat. Number TRS-VATS-15: 201808085

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1307-2019%22

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