Public recall detail

TARO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution

2026-02-09

medium
Drugs Product quality
Quick summary

Quick summary: TARO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution . Reason: Product quality. Category: Drugs. Date: 2026-02-09.

Recommended action

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

Recall details

Quick summary: TARO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution . Reason: Product quality. Category: Drugs. Date: 2026-02-09.

Official details

Affected product details

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

BrandTaro, TARO, RAN
ProductTARO-CANDESARTAN
IssueHealth products - Product quality
Recall classType II
IdentificationRA-81592

Affected products

BrandTARO
ProductTARO-CANDESARTAN
DIN / NPN / authorizationDIN 02380684
Dosage formTablet
StrengthCANDESARTAN CILEXETIL 4 MG
LotPTG4320A PTG4321A
BrandTARO
ProductTARO-CANDESARTAN
DIN / NPN / authorizationDIN 02380692
Dosage formTablet
StrengthCANDESARTAN CILEXETIL 8 MG
LotPTF3333A PTF3338A PTF5487A PTF5488A PTF5489A PTF5490A PTF5491A PTF6159A PTG1103A PTG1083A
BrandTARO
ProductTARO- CANDESARTAN
DIN / NPN / authorizationDIN 02380706
Dosage formTablet
StrengthCANDESARTAN CILEXETIL 16 MG
LotPTF3339A PTF5498A PTF5497A PTG1386A PTG1387A PTG1388A
BrandRAN
ProductRAN-CANDESARTAN
DIN / NPN / authorizationDIN 02380714
Dosage formTablet
StrengthCANDESARTAN CILEXETIL 32 MG
LotPTF3279A PTF3280A PTF3281A PTF3282A PTF3283A

Issue

Affected lots were manufactured using an active ingredient that was out of specification for dissolution.

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 Healthcare Industry
CategoryHealth products - Drugs
CompaniesSUN PHARMA CANADA INC 126 East Drive Brampton, ON L6T 1C1
DistributionNational
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-81592
Background{}
CompaniesSUN PHARMA CANADA INC 126 East Drive Brampton, ON L6T 1C1
AudiencesGeneral public Healthcare Industry
Source updated2026-02-09

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

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