Medtronic recalls Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling system 30 mm Vascular/Medium. Missing sled component may cause staple line failure, leading to bleeding or leakage.
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 Tri-Staple 2.0 Curved Tip Intelligent Reload surgical staples because a missing sled component could cause staple deployment failure. This might lead to bleeding or leakage of bodily fluids during surgery.
The device may be missing a critical sled component that guides staple deployment. Without this part, the staples might not form properly when dividing tissue, potentially causing bleeding or leakage of bodily fluids.
Surgical patients and medical professionals using the Tri-Staple 2.0 Curved Tip Intelligent Reload with Signia stapling system 30 mm Vascular/Medium. Those at highest risk are patients undergoing procedures requiring this specific staple type.
Check for the item code SIG30ACTAVM or N7L1163X/N7M0156X on the product packaging. This specific staple is used with the Signia stapling system 30 mm Vascular/Medium.
Look for item codes SIG30ACTAVM, N7L1163X, or N7M0156X on the packaging or label.
The recall applies to specific surgical staples used in procedures requiring the Signia stapling system 30 mm Vascular/Medium. If you have the listed item codes, contact Medtronic for guidance.
Check the item code on the packaging: SIG30ACTAVM, N7L1163X, or N7M0156X. This specific staple is used with the Signia stapling system 30 mm Vascular/Medium.
The recall does not specify a remedy. Check with Medtronic directly for instructions on handling the affected product.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-2514-2018 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-2514-2018 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.
