Imipenem And Cilastatin For Injection 500 Mg/500 Mg Single-dose Vials - Incorrect Labelling Information

Recall Summary Imipenem and Cilastatin for Injection 500 mg/500 mg vials distributed across Canada have incorrect information on their labels. The labeling error poses a product safety concern. This recall affects healthcare facilities and providers who use this antibiotic medication.

Reason
Product safety
Category
drug recall
Country
Canada
Agency
HC-DRUGS
Recall date
2016-09-06
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DRUGS

Recall details on Nibble Recalls: https://trynibble.app/recalls/fa731c35-e282-476e-b525-c92ef77ebdf3