Medtronic recalls Endo GIA universal staplers with possible missing sled component that could cause staple line failure, leading to bleeding or leakage during surgery. Affected models include GK3, GK4, and others.
Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding or leakage of luminal contents.
Medtronic is recalling certain Endo GIA universal staplers that may have a missing sled component. This could cause staple lines to fail during surgery, potentially leading to bleeding or leakage of internal tissues.
The sled component is critical for deploying staples properly. If missing, the stapler may fail to form a secure staple line when dividing tissue, which could cause bleeding or leakage of internal contents during surgery.
Surgical teams using the recalled Endo GIA staplers for gastrointestinal procedures are most at risk. Patients undergoing surgery with these devices could experience complications.
Check for model numbers GK3, GK4, or JAWI on the product label. These staplers were sold with specific lot numbers listed in the recall notice.
Look for model numbers GK3, GK4, or JAWI on the device label to confirm if it is affected.
Reach out to Medtronic directly for further assistance with the recall.
The sled component may be missing, which can cause staple line failure during surgery, leading to bleeding or leakage of internal tissues.
Endo GIA universal staplers with model numbers GK3, GK4, or JAWI.
Check the product label for model numbers GK3, GK4, or JAWI, and verify against the listed lot numbers in the recall notice.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-1859-2018 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1859-2018 from Medtronic. 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.
