Home/Recalls/CANADA-RA-76691
Health CanadaType II

Baciject (Bacitracin for Injection USP) 50,000 units per vial (2021-10-20)

Published: October 20, 2021Recall ID: RA-76691Category: generalCountry: Canada

Product Description & Identification

Baciject (Bacitracin for Injection USP) 50,000 units per vial (2021-10-20)

Additional Source Details

FieldValue
Panels › 1 › Text<b>Issue:</b> Product Safety<BR/><b>Audience:</b> General Public, Healthcare Professionals, Hospitals<BR/><b>Category:</b> Drugs<BR/><b>Alert type:</b> Drug Recall<BR/><b>Department:</b> Health Canada<BR/><b>Hazard classification:</b> Type II<BR/>
Panels › 1 › TitleSummary
Panels › 1 › Panel Namebasic_details
Panels › 2 › Text<b>Product: </b>Baciject 50,000 Units/Vial<BR/>
Panels › 2 › TitleSummary
Panels › 2 › Panel Namesummary
Panels › 3 › Text 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.
Panels › 3 › TitleReason
Panels › 3 › Panel Namecms_reason_reason_recall
Panels › 4 › Text Retailers, Wholesalers
Panels › 4 › TitleDepth of distribution
Panels › 4 › Panel Namecms_reason_depth_distribution
Panels › 5 › Text<b>Brand name:</b> Baciject 50,000 Units/Vial<br/><b>Dosage form:</b> Powder for solution<BR/><b>Strength:</b> Bacitracin 50000 Unit/Vial<BR/><b>DIN, NPN, DIN-HIM:</b> DIN 02245571<BR/><b>Lot or serial number:</b> AK2184, AL1233, AM1790<BR/><b>Companies:</b><br/><dl><dt>Recalling Firm</dt><dd>Sterimax Inc.</dd><dd>2770 Portland Drive</dd><dd>Oakville</dd><dd>L6H 6R4</dd><dd>Ontario</dd><dd>CANADA</dd></dl><dl><dt>Marketing Authorization Holder</dt><dd>Sterimax Inc.</dd><dd>2770 Portland Drive</dd><dd>Oakville</dd><dd>L6H 6R4</dd><dd>Ontario</dd><dd>CANADA</dd></dl>
Panels › 5 › TitleBaciject 50,000 Units/Vial
Panels › 5 › Panel Nameproduct_1
Panels › 6 › Text<b>Identification number:</b> RA-76691<BR/>
Panels › 6 › TitleIdentification number
Panels › 6 › Panel Nameid_numbers
Recall IdRA-76691
Start date1634688000
Date published-62169984000

Overview

  • Risk LevelType II
Official Agency Alert