FDAFDA · Food and drugs·Recall number Z-1419-2021
Covidien Tri-Staple 2.0 Reinforced Intelligent Reload 60 mm Medium/Thick-For use with Signia stapling system. Staple line reinforcement has applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection of tissue and creation of anastomosis. It may be used for transection and resection of liver substance, hepatic vasculature and biliary structures, and for transection and resection of pancreas. Product Number: SIGTRSB60AMT
Published April 21, 2021 · Recall initiated: March 23, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Potential for the pouch to contain an extra laminate layer, creating the potential for the device sterility to be compromised. The inclusion of an additional laminate layer in the package may also impact complete de-gassing of the sterilization gas, Ethylene Oxide and may result in a potentially increased risk for patient infection and/or potential exposure to Ethylene Oxide retained in the pouch
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Covidien Llc
- Distributor
- AL, AR, FL, IN, LA, MA , MN, MO, NJ, NY, OR, PA, TX
- Lot
- Lot Number: N0M0801RY Exp. Date: ¿11/30/2023 UDI: A8845217176201 20884521717623
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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