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