medical Class II Updated 2020-06-10

Covidien Llc recalls Multifire VersaTrack Auto Suture Hernia Stapler, 4.8mm, Part

Recalled Product

Multifire VersaTrack Auto Suture Hernia Stapler, 4.8mm, Part No. 174023 - 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).


Hazard / Issue

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.

Issued by

FDA

Distribution: Worldwide distribution.
Lot/Code Info: Lots P9J1172Y P9K0452Y P9K0453Y P9K0454Y P9K1596Y P0B0996Y
View official government recall

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