Quick summary: VENLAFAXINE XR: out of specification. Reason: Product quality. Category: Drugs. Date: 2026-03-10.
Public recall detail
VENLAFAXINE XR: out of specification
2026-03-10
Drugs
Product quality
Quick summary
Recommended action
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: VENLAFAXINE XR: out of specification. Reason: Product quality. Category: Drugs. Date: 2026-03-10.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandPro-Doc Lté, VENLAFAXINE XR
ProductVENLAFAXINE XR 75mg
IssueHealth products - Product quality
Recall classType II
IdentificationRA-81722
Affected products
BrandVENLAFAXINE XR
ProductVENLAFAXINE XR
DIN / NPN / authorizationDIN 02339250
Dosage formCapsule (extended release)
StrengthVenlafaxine (Venlafaxine Hydrochloride) 75mg
Lot2505003230
Issue
Dissolution is out of specification in the affected batch.
What you should do
- Verify if your product is affected.
- Consult your healthcare provider prior to discontinuing use of the affected product, or for any health concerns.
- 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
AudienceGeneral public Healthcare Industry
CategoryHealth products - Drugs
CompaniesPro-Doc Lté. 2925 boul. Industriel, Laval, Qc, H7L 3W9
Recall date2026-03-10
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-81722
Background{}
CompaniesPro-Doc Lté. 2925 boul. Industriel, Laval, Qc, H7L 3W9
AudiencesGeneral public Healthcare Industry
Source updated2026-03-10
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
FAQ
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