Public recall detail

Uniprim Oral Powder: Packaging defect in affected lots

2026-11-03

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Health products Health product recall
Quick summary

Quick summary: Uniprim Oral Powder: Packaging defect in affected lots. Reason: Health product recall. Category: Health products. Date: 2026-11-03.

Recommended action

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

Recall details

Quick summary: Uniprim Oral Powder: Packaging defect in affected lots. Reason: Health product recall. Category: Health products. Date: 2026-11-03.

Official details

Affected product details

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

Branduniprim, Uniprim Oral Powder
ProductNeogen Vet Uniprim Oral Powder (Apple Flavored)
IssueHealth products - Packaging
Recall classType III
IdentificationRA-82895

Affected products

BrandUniprim Oral Powder
ProductNeogen Vet Uniprim Oral Powder (Apple Flavored)
DIN / NPN / authorizationDIN 02241375
Dosage formPowder
StrengthSulfadiazine 333mg/g Trimethoprim 67mg/g
LotCAUP0128261CC CAUP0202261CC CAUP0203261CC CAUP0421261CC CAUP0422261CC CAUP0423261CC CAUP0825261CC CAUP0826261CC CAUP0827261CC

Issue

Packaging defect may compromise container closure integrity in the affected lots.

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 - Veterinary drugs
CompaniesNeogen Corporation1847 Mercer Road, Suite A, Lexington, Kentucky, 40511, USA
DistributionNational
Published byHealth Canada
Recall classType III
Alert / recall typeHealth product recall
Identification numberRA-82895
Background{}
CompaniesNeogen Corporation1847 Mercer Road, Suite A, Lexington, Kentucky, 40511, USA
AudiencesGeneral public Healthcare Industry
Source updated2026-11-04

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

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