TiLoop Mesh (2020-04-10)
- Starting date:
- April 10, 2020
- Posting date:
- April 24, 2020
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-72865
Last updated: 2020-04-24
Affected Products
TiLoop Mesh
Reason
Medical Device License 77410 for the TiLoop Mesh has been suspended by Health Canada.
Affected products
TiLoop Mesh
Lot or serial number
All lots.
Model or catalog number
- 6000636
- 6000637
- 6000638
- 6000639
- 6000640
- 6000641
Companies
- Manufacturer
-
PFM Medical Inc.
1916 Palomar Oaks Way, Suite 150
Carlsbad
92008
California
UNITED STATES