FDA Device recall Z-2255-2020
Multifire Endo Hernia 0 12mm Stapler with 4.0mm Disposable Loading Unit , Part No. 174027 - Product Usage: has application in endoscopic ge…
- FDA Device
- Class II
- ongoing
- Published 2020-06-10
On 2020-06-10 the FDA classified a Class II recall of Multifire Endo Hernia 0 12mm Stapler with 4.0mm Disposable Loading Unit , Part No. 174027 - Product Usage: has application in endoscopic ge… by Covidien, citing 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 comp….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2255-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-05-12 |
| Published | 2020-06-10 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Covidien |
| Distribution | n/a |
Product
Multifire Endo Hernia 0 12mm Stapler with 4.0mm Disposable Loading Unit , Part No. 174027 - Product Usage: has application in endoscopic general surgery procedures for fixation of mesh in the repair of hernial defects and in other surgical specialties for approximation of tissue(s).
Reason
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.
Identifiers
| code_info | Lots P9J0368Y P9J0369Y P9J0517Y P9K1300Y |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2255-2020%22
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