Reported May 15, 2019 · Terminated

ConMed Anchor Tissue Retrieval System 10 MM, 235 ML, (5/BX) Catalog Number: TRS100SB2 The Anchor Tissue Retrieval…

Conmed Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Conmed Corporation · 310 Broad St · Utica, NY · 13501-1203

Is this the product you have?

    • ConMed Anchor Tissue Retrieval System 10 MM
    • 235 ML
    • (5/BX)
  • Catalog NumberTRS100SB2 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
Lot codes and dates

3 of 3 products

Products covered by this recall
#Product as published
1All alpha/numeric lot codes (e.g. lots 68A8T or 19A8T)
2All numeric lot codes ending with the number 9 (e.g. Lot code 201902159)
3All excluded numeric lot codes listed in the tables below for each specific catalog number: Excluded Lot Codes for Cat. Number TRS100SB2: 201805095 201806055 201809265 201810314 201811224 201812114 201805144 201806115 201809285 201811054 201811234 201812124 201805145 201807134 201810014 201811064 201811264 201812144 201805194 201807245 201810094 201811074 201811274 201812174 201805214 201808155 201810154 201811084 201811284 201812184 201805255 201808164 201810164 201811124 201811304 201812204 201805284 201808165 201810184 201811134 201812034 201812214 201805295 201808205 201810194 201811144 201812044 201901024 201805315 201808214 201810224 201811154 201812054 201901034 201806015 201808225 201810234 201811164 201812064 201901044 201806045 201808234 201810244 201811204 201812074 201901074 201806054 201809255 201810254 201811214 201812104
Amount recalled
69385

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

  • Nationwide

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jan 17, 2023 · Data as of Sep 19, 3:38 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.