CanadaAA Pharma Inc’s KETOROLAC solution (Ketorolac Tromethamine 0.5% w/v), DIN 02245821, lots VE3252 and VE3251 is affected. It was recalled because the weight is out of specification; verify if your product is one of the affected lots, consult your healthcare provider before discontinuing use, contact the recalling firm with questions, and report any side effects or other safety complaints to Health Canada.
What's being recalled
Depth of recall: Retailers
Companies: AA Pharma Inc., 1165 Creditstone Road, Unit #1,, Vaughan, ON,, L4K 4N7.
How to identify it
Brand: KETOROLAC; Product Name: KETOROLAC; Market Authorization: DIN 02245821; Dosage Form: Solution; Strength: Ketorolac Tromethamine 0.5% w/v; Lot: VE3252, VE3251
The hazard
The weight is out of specification in the affected lots.
What to 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.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)