Pds Plus Antibacterial Suture Cl, Vl And Vl (loop) (2019-12-23)

PDS Plus Antibacterial Suture Recall PDS Plus Antibacterial Suture products in CL, VI, and VI (Loop) versions are being recalled across Canada. The recall is classified as Class I, meaning there is a serious risk of injury or death. The specific reason for the recall relates to issues with the medical device itself, though detailed technical information is not provided in this notice.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-01-10
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1e89420f-d7e4-48a9-ad6b-7d6337d73c5c