Stimuplex Ultra 360 Insulated Echogenic Needle And Ultraplex 360 Non-stimulating Echogenic Needle (2018-09-24)

Recall Summary Stimuplex Ultra 360 Insulated Echogenic Needles and Ultraplex 360 Non-Stimulating Echogenic Needles are being recalled across Canada due to a medical device issue. These needles are used in medical procedures for nerve blocks and regional anesthesia. The recall affects healthcare facilities and medical professionals who have these products in stock.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-10-19

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/8b20aeda-9ba0-4927-8c55-f7c0f29a0c67