Covidien recalls Multifire VersaTrack Auto Suture Hernia Stapler (4.0mm, Part No. 174021) due to a manufacturing error that may cause staples to fail advancing when handle is compressed. Affected lots: P9J0241Y, P9J0242Y, P9J0243Y, P9K1140Y, P9K1663Y, P9K1141Y.
The product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly advance within the staple cartridge when the instrument handle is compressed.
Covidien is recalling a specific model of hernia stapler used in endoscopic surgery because a manufacturing error might cause staples to not advance properly when the handle is pressed. This could lead to improper surgical repairs if the device is used without fixing the issue.
The stapler's staples may not advance correctly when the handle is compressed due to a manufacturing assembly error. This could result in improper tissue fixation during surgery, potentially causing surgical complications.
Surgical professionals who use this stapler for hernia repairs or other endoscopic procedures are most at risk. Patients undergoing surgery with this device may also be affected if the stapler malfunctions.
Check for the product name 'Multifire VersaTrack Auto Suture Hernia Stapler', 4.0mm size, and part number 174021. Affected lots are P9J0241Y, P9J0242Y, P9J0243Y, P9K1140Y, P9K1663Y, and P9K1141Y.
Identify the lot number on the device, which should be one of P9J0241Y, P9J0242Y, P9J0243Y, P9K1140Y, P9K1663Y, or P9K1141Y.
Reach out to Covidien for further instructions on how to address the issue, as the recall remedy is not specified in the record.
The recall indicates a potential issue that could cause staples to fail advancing when the handle is compressed, so it is not recommended for use until the manufacturer provides instructions.
Check the lot number to see if it's affected. If it is, contact Covidien for guidance on next steps, as the recall remedy is not specified in the record.
Look for the product name 'Multifire VersaTrack Auto Suture Hernia Stapler', 4.0mm size, and part number 174021 with one of the affected lot numbers: P9J0241Y, P9J0242Y, P9J0243Y, P9K1140Y, P9K1663Y, or P9K1141Y.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2252-2020 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2252-2020 from Covidien. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
