Certain Bottles Of Jamp Venlafaxine Xr 37.5 Mg Capsules Recalled Due To Mislabelling That Could Lead To Overdose
JAMP Venlafaxine XR 37.5 mg capsules in lot PTC5140A are being recalled in Canada because the bottles are mislabeled, which could result in patients taking incorrect doses. The affected product was distributed to pharmacies in 100-capsule bottles for dispensing to patients. This recall applies to bottles distributed across Canada.
- Product
- JAMP Venlafaxine XR 37.5 mg (lot PTC5140A) sold to pharmacies in bottles of 100 capsules for dispensing.
- Reason
- Labelling
- Category
- consumer product recall
- Country
- Canada
- Agency
- HC-PRODUCTS
- Recall date
- 2023-06-21
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-PRODUCTS
Recall details on Nibble Recalls: https://trynibble.app/recalls/ddfd548b-2031-4780-9eee-c3e4d9d8456f