FOLLTROPIN-V (VETOQUINOL), DIN 00867357, Powder for Solution, FSH 400 mg/vial — lots 510125, 510127, 510573, 510574, 713591 and 713592 sold nationally in Canada — is affected. It was recalled because the vial of sterile diluent in these lots may contain particulate matter; verify if your product is affected, consult your healthcare provider before discontinuing use, contact Vetoquinol N.-A. Inc. with questions, and report any side effects or other safety complaints to Health Canada.
What's being recalled
Depth of recall: Health Care Establishments
Companies: Vetoquinol N.-A. Inc., 2000 Chemin Georges, Lavaltrie, QC, J5T 3S5.
How to identify it
Brand: VETOQUINOL; Product Name: FOLLTROPIN-V; Market Authorization: DIN 00867357; Dosage Form: Powder For Solution; Strength: FOLLICLE STIMULATING HORMONE (FSH) 400 MG / VIAL; Lot numbers: 510125, 510127, 510573, 510574, 713591 & 713592
The hazard
The vial of sterile diluent in the affected lots may contain particulate matter.
What to 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.
Where it was sold
National
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)