Restorelle Polypropylene Mesh (2019-07-11)

Restorelle Polypropylene Mesh Recall Summary Restorelle Polypropylene Mesh, a medical device used in surgical procedures, has been recalled across Canada. The recall is classified as Class I, indicating a serious issue with the product. The specific reason for the recall relates to concerns with the medical device itself, affecting all patients and healthcare facilities that received this product in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-07-26
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4426a0f0-bff1-4d1d-835a-b63a477c30e6