Health product recall

Multifire VersaTack Auto Suture Hernia Stapler 4.0 mm and Multifire VersaTack Auto Suture Hernia Stapler 4.8 mm & Multifire Endo Hernia Auto Suture Straight Hernia Stapler12mm- 4.8 mm and Multifire Endo Hernia Auto Suture Straight Hernia Stapler12mm-...

Starting date:
May 15, 2020
Posting date:
June 5, 2020
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-73251

Last updated: 2020-06-05

Affected Products

A. Multifire VersaTack Auto Suture Hernia Stapler 4.0 mm and Multifire VersaTack Auto Suture Hernia Stapler 4.8 mm
B. Multifire Endo Hernia Auto Suture Straight Hernia Stapler12mm- 4.8 mm and Multifire Endo Hernia Auto Suture Straight Hernia Stapler12mm- 4.0 mm

Reason

Recall due to manufacturing assembly error.

Affected products

A. Multifire VersaTack Auto Suture Hernia Stapler 4.0 mm and Multifire VersaTack Auto Suture Hernia Stapler 4.8 mm

Lot or serial number
  • P9J0241Y
  • P9J1172Y
  • P9K0452Y
  • P9K0454Y
  • P9K1596Y
Model or catalog number
  • 174021
  • 174023
Companies
Manufacturer
Covidien LLC
15 Hampshire Street
Mansfield
02048
Massachusetts
UNITED STATES

B. Multifire Endo Hernia Auto Suture Straight Hernia Stapler12mm- 4.8 mm and Multifire Endo Hernia Auto Suture Straight Hernia Stapler12mm- 4.0 mm

Lot or serial number
  • P9J0368Y
  • P9J0369Y
  • P9J0517Y
  • P9J1171Y
  • P9K1395Y
Model or catalog number
  • 174025
  • 174027
Companies
Manufacturer
Covidien LLC
15 Hampshire Street
Mansfield
02048
Massachusetts
UNITED STATES