Lithotripsy Probe 1.9fr 375cm (2019-06-20)

Recall Summary A Lithotripsy Probe 1.9FR 375cm has been recalled across Canada due to a medical device issue. This device was distributed nationally and classified as a Class I recall, indicating a serious safety concern. The recall affects all units of this specific lithotripsy probe model.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-07-05

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/426e0ae6-2e69-4703-9b98-ae1711f8206c