Oxoid Nitrocefin (2016-03-15)

OXOID NITROCEFIN Recall Summary OXOID Nitrocefin, a medical device product, has been recalled across Canada due to quality or safety concerns that warranted a Class I classification. This recall affects all Canadian consumers and healthcare facilities that have received this product. The specific nature of the defect or risk associated with Nitrocefin has not been detailed in the available information.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-04-15
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ca9b480c-7665-49ed-afd0-fd112b45f6aa