Covidien recalls Multifire Endo Hernia 0 12mm Stapler with 4.0mm Loading Unit (Lots P9J0368Y, P9J0369Y, P9K1:1300Y) due to a manufacturing error that may cause staples to fail advancing during use in endoscopic surgery.
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 endoscopic hernia stapler used in surgery because a manufacturing error might cause staples to not advance properly when the handle is pressed. This could lead to improper tissue fixation during procedures.
The stapler has a manufacturing defect that may cause staples to fail to advance into the cartridge when the handle is compressed. This could result in improper tissue fixation during surgery, potentially leading to incomplete repairs.
Surgical teams using the recalled stapler for endoscopic hernia repairs or tissue approximation. The risk is highest for surgeons and surgical staff handling the specific lot numbers.
Check for the product name 'Multifire Endo Hernia 0 12mm Stapler with 4.0mm Disposable Loading Unit' and part number 174027. The affected lots are P9J0368Y, P9J0369Y, and P9K1300Y.
Look for the lot numbers P9J0368Y, P9J0369Y, or P9K1300Y on the packaging or instrument.
The recall states the product may have a manufacturing error that could cause staples to fail advancing during use, but the remedy is not specified in the record.
The recall record does not provide a remedy, so no specific action is required beyond checking the lot number.
Check for the product name and part number 174027 with the affected lot numbers: P9J0368Y, P9J0369Y, or P9K1300Y.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2255-2020 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2255-2020 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.
