Endo GIA" Radial Reload with Tri-Staple" Technology The recall
Endo GIA" Radial Reload with Tri-Staple" Technology The Endo GIA radial reloads with Tri-Staple Technology have application in open or minimally…
Why was Endo GIA" Radial Reload with Tri-Staple" Technology The recalled?
The device cartridge disengaged during use due to manufacturing error.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Product number: EGIARADXT Lot code: N6L0351X
- Product
- Endo GIA" Radial Reload with Tri-Staple" Technology The Endo GIA radial reloads with Tri-Staple Technology have application in open or minimally…
- Recalling firm
- Covidien LLC
- Quantity
- 163
- Distribution
- Internationally, including Japan. No USA Customers
- Recall date
- March 14, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)