Summary

Issue: Product Safety
Audience: General Public, Healthcare Professionals, Hospitals
Category: Drugs
Alert type: Drug Recall
Department: Health Canada
Hazard classification: Type II

Summary

Product: Baciject 50,000 Units/Vial

Reason

The barcode on the vial label of Baciject injection was incorrect for the affected lots; the barcode corresponds to a different Sterimax product, Phenylephrine hydrochloride injection.

Depth of distribution

Retailers, Wholesalers

Baciject 50,000 Units/Vial

Brand name: Baciject 50,000 Units/Vial
Dosage form: Powder for solution
Strength: Bacitracin 50000 Unit/Vial
DIN, NPN, DIN-HIM: DIN 02245571
Lot or serial number: AK2184, AL1233, AM1790
Companies:

Recalling Firm

Sterimax Inc.

2770 Portland Drive

Oakville

L6H 6R4

Ontario

CANADA

Marketing Authorization Holder

Sterimax Inc.

2770 Portland Drive

Oakville

L6H 6R4

Ontario

CANADA

Identification number

Identification number: RA-76691