Recall Z-2252-2020

Covidien Llc · initiated May 12, 2020

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Multifire VersaTrack Auto Suture Hernia Stapler, 4.0mm, Part No. 174021 - 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).

Codes / lots: Lots P9J0241Y P9J0242Y P9J0243Y P9K1140Y P9K1663Y P9K1141Y

Reason for recall

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.

FDA-determined cause: Process control

Action taken

All consignees were notified by letter titled "Urgent Medical Device Recall" delivered via Federal Express and/or certified mail beginning May 12, 2020. The letter informs customers of the recall of specific item codes and production lots of Multifire hernia staplers due to a manufacturing assembly error. Use of a device with this condition may result in the failure of staples to properly advance within the staple cartridge when the instrument handle is compressed. Customers are instructed to take the following actions: " Immediately quarantine and discontinue use of the affected item code and lot. " Return affected product. " Promptly forward the information from the customer communication to any recipients to whom they have distributed any of the affected product. " Complete the Recalled Product Return Form even if you do not have inventory. If you have any questions about this event, you may contact Medtronic via email at rs.assurancequality@medtronic.com

Details

Recall number
Z-2252-2020
Initiated
May 12, 2020
Product code
GCI – Laryngoscope, Endoscope
Quantity
12,610 total
Distribution
Worldwide distribution.
Recalling firm
Covidien Llc, Mansfield, MA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-2253-2020 Class IIMultifire VersaTrack Auto Suture Hernia Stapler, 4.8mm, Part No. 174023 - Product Usage:…The product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly… 05/12/2020Open, Classified
Z-2254-2020 Class IIMultifire Endo Hernia 0 12mm Stapler with 4.8mm Disposable Loading Unit , Part No.…The product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly… 05/12/2020Open, Classified
Z-2255-2020 Class IIMultifire Endo Hernia 0 12mm Stapler with 4.0mm Disposable Loading Unit , Part No.…The product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly… 05/12/2020Open, Classified