Multifire Endo Hernia 0 12mm Stapler with 4.8mm recall
Multifire Endo Hernia 0 12mm Stapler with 4.8mm Disposable Loading Unit , Part No. 174025 - Product Usage: has application in endoscopic general…
Why was Multifire Endo Hernia 0 12mm Stapler with 4.8mm recalled?
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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
Lots P9J1171Y P9K1395Y P9K1582Y
- Product
- Multifire Endo Hernia 0 12mm Stapler with 4.8mm Disposable Loading Unit , Part No. 174025 - Product Usage: has application in endoscopic general…
- Recalling firm
- Covidien Llc
- Quantity
- 12,610 total
- Distribution
- Worldwide distribution.
- Recall date
- June 10, 2020
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)