Health product recall

Heparin Sodium Injection: Out of Specification

Dernière mise à jour

Summary

Produit
HEPARIN SODIUM INJ IN 5% DEX 100UNITS/ML
Problème
Health products - Product quality
Ce qu’il faut faire

Consult your health care professional if you have any health concerns.

Affected products

Brand

Product Name

Market Authorization

Dosage Form

Strength

Lot

HEPARIN SODIUM INJ IN 5% DEX 100UNITS/ML

HEPARIN SODIUM INJ IN 5% DEX 100UNITS/ML

DIN 02209721

Solution

Heparin Sodium 10,000 UNITS/100 ML,
Dextrose 5 G/100 ML

J2A262

Problème

Potential low Anti-Factor Ila potency out of specification.

Ce que vous devriez faire

  1. Verify if your product is affected.
  2. Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
  3. Contact the recalling firm if you have any questions about the recall.
  4. Report any health product related side effects to Health Canada.
  5. Report any other health product safety complaints to Health Canada.

Additional information

Contexte

Depth of recall: Wholesalers, Retailers, End Users

Details
Original published date: 2023-03-01
Type d’avis ou de rappel
Health product recall
Catégorie
Health product - Drugs
Entreprises

B. Braun Medical Inc.
2525 McGaw Ave, Irvine CA, United States

Published by
Health Canada
Audience
General public
Healthcare
Industry
Classe de rappel
Type II
Identification number
RA-73062