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Health CanadaType II

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

Veröffentlicht: 20. Oktober 2021Rückruf-ID: RA-76691Kategorie: VerbraucherprodukteLand: Kanada
Canada
Safety AlertHealth CanadaCanadaCanada

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

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Produktbeschreibung & Identifikation

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

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Check the model number, serial number, and date stamp on the rating label on the back or underside of the product.

2Isolate & Discontinue Use

Immediately discontinue using the product. Unplug electrical items and keep juvenile items out of reach of children.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (Health Canada).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought Baciject (Bacitracin for Injection USP) 50,000 units per vial (2021-10-20)?

Immediately stop using the product and keep it out of reach of children. Disconnect power if electrical, and do not attempt makeshift home repairs.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (Health Canada). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Übersicht

  • RisikostufeType II
Recall Hazard Severity
Caution (Class III)
Offizielle Behördenwarnung

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

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