COVIDIEN MEDTRONIC Recall: Endo GIA 45 mm Articulating Medium/Thick Reload with Tri-Staple
COVIDIEN MEDTRONIC Recall: Endo GIA 45 mm Articulating Medium/Thick Reload with Tri-Staple is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: COVIDIEN MEDTRONIC; Product: Endo GIA 45 mm Articulating Medium/Thick Reload with Tri-Staple Technology, Item Code EGIA45AMT; Reason for recall: De
| Recalling firm | COVIDIEN MEDTRONIC |
|---|---|
| Product | Endo GIA 45 mm Articulating Medium/Thick Reload with Tri-Staple Technology, Item Code EGIA45AMT |
| Reason for recall | 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. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Nationwide U.S.A. Internationally to: Albania, Algeria, Austria, Belgium, Bulgaria, Croatia, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Guadeloupe, Hungary, Iceland, Ireland, Israel, Italy, Ivory Coast, Jordan, Kazakhstan, Kuwait, Latvia, Lebanon, Luxembourg, Macedonia, Malt |
| Recall initiated | 20180522 |
| Recall number | Z-2503-2018 |
| Category | device |
| State | CT |
| Country | United States |
$29/mo
Try RecallGuard →