Quick summary: Reddy-Dasatinib: out of specification. Date: 2022-01-31.
Public recall detail
Reddy-Dasatinib: out of specification
2022-01-31
Recall
Safety notice
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: Reddy-Dasatinib: out of specification. Date: 2022-01-31.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandReddy-Dasatinib
ProductReddy-Dasatinib
IssueHealth products - Product quality
Recall classType III
IdentificationRA-63870
Affected products
BrandReddy-Dasatinib
ProductReddy-Dasatinib
DIN / NPN / authorizationDIN 02514796
Dosage formTablet
StrengthDASATINIB (Dasatinib (S)-propylene glycol) 140 mg
LotZH10018, ZH10019
Issue
The dissolution is out of specification in the affected lot(s).
What you should do
- Verify if your product is affected.
- Consult your healthcare provider prior to discontinuing use of the affected product(s), 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 Health professionals Hospitals
CategoryHealth products - Drugs
CompaniesDr. Reddy's Laboratories Canada Inc. 5580 Explorer Drive, Suite 204, Mississauga, Ontario, L4W 4Y1
Published byHealth Canada
Recall classType III
Alert / recall typeHealth product recall
Identification numberRA-63870
Background{}
CompaniesDr. Reddy's Laboratories Canada Inc. 5580 Explorer Drive, Suite 204, Mississauga, Ontario, L4W 4Y1
AudiencesGeneral public Health professionals Hospitals
Source updated2022-01-31
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
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