Public recall detail

Dextrose 50 mg/mL Injection; Out of Specification

2023-05-31

medium
Recall Safety notice
Quick summary

Quick summary: Dextrose 50 mg/mL Injection; Out of Specification. Date: 2023-05-31.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Dextrose 50 mg/mL Injection; Out of Specification. Date: 2023-05-31.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandICU Medical Canada
ProductDextrose 50 mg/mL Injection USP
IssueHealth products - Product quality
Recall classType II
IdentificationRA-73732

Affected products

BrandICU Medical Canada
ProductDextrose 50 mg/mL Injection USP
DIN / NPN / authorizationDIN 00037915
Dosage formSolution
StrengthDextrose 50 mg / mL
Lot5781810

Issue

The dextrose content is out of specification in the affected lot.

What you should do

  • Verify if your product is affected.
  • Contact the recalling firm if you have any questions about the recall.
  • Report any health product related side effects to Health Canada.
  • Report any other health product safety complaints to Health Canada.
Additional official information
AudienceHealthcare Industry
CategoryHealth products - Drugs
CompaniesICU Medical Canada Inc. 2600 Alfred-Nobel boul., Suite 100, Montréal, QC, H4S 0A9 Canada
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-73732
Background{}
CompaniesICU Medical Canada Inc. 2600 Alfred-Nobel boul., Suite 100, Montréal, QC, H4S 0A9 Canada
AudiencesHealthcare Industry
Source updated2023-05-31

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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