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Ketorolac Recalled Due to Weight Out of Specification

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Published March 9th, 2026
Detected March 10th, 2026
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Summary

Health Canada has issued a Type II recall for Ketorolac (DIN 02245821) manufactured by AA Pharma Inc. due to weight being out of specification in affected lots VE3252 and VE3251. Retailers are instructed on the recall process and consumers are advised to consult healthcare providers.

What changed

Health Canada, through AA Pharma Inc., has initiated a recall for specific lots (VE3252, VE3251) of KETOROLAC (DIN 02245821) due to the product's weight being out of specification. This recall is classified as a Type II, indicating a lower risk to health, but still requires immediate attention from affected parties.

Retailers are directed to verify affected products and manage the recall process. Consumers are advised to consult their healthcare provider before discontinuing use of the product and to report any health product-related side effects or safety complaints to Health Canada. The recalling firm, AA Pharma Inc., should be contacted for any questions regarding the recall.

What to do next

  1. Verify if affected Ketorolac lots (VE3252, VE3251) are in inventory.
  2. Remove affected product from shelves and follow recall procedures.
  3. Advise consumers to consult healthcare providers regarding the recalled product.

Source document (simplified)

Health product recall

KETOROLAC: The weight is out of specification in the affected lots.

Brand(s)

AA Pharma Inc

Last updated

2026-03-09

Summary

Product KETOROLAC Issue Health products - Product quality What to do Consult your healthcare provider prior to discontinuing use of the affected product, or for any health concerns.

Affected products

| Brand | Product Name | Market Authorization | Dosage Form | Strength | Lot |
| --- | --- | --- | --- | --- | --- |
| KETOROLAC | KETOROLAC | DIN 02245821 | Solution | Ketorolac Tromethamine 0.5% w/v | VE3252, VE3251 |

Issue

The weight is out of specification in the affected lots.

What you should do

  1. Verify if your product is affected.
  2. Consult your healthcare provider prior to discontinuing use of the affected product, or for any health concerns.
  3. Contact the recalling firm if you have any questions about the recall.
  4. Report any health product related side effects to Health Canada.
  5. Report any other health product safety complaints to Health Canada.

Additional information

Background

Depth of recall: Retailers

Details

Original published date:

2026-03-09

Alert / recall type Health product recall Category Health products - Drugs Companies

AA Pharma Inc.

1165 Creditstone Road, Unit #1,

Vaughan, ON,

L4K 4N7

Published by Health Canada Audience General public Healthcare Industry Recall class Type II Recall date

2026-03-09

Identification number RA-81716

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Source

Analysis generated by AI. Source diff and links are from the original.

Classification

Agency
Various Canadian Agencies
Published
March 9th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Substantive

Who this affects

Applies to
Drug manufacturers Healthcare providers Retailers
Geographic scope
National (CA)

Taxonomy

Primary area
Product Safety
Operational domain
Compliance
Topics
Pharmaceuticals Recalls

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