Venlafaxine Hydrochloride recall: Failed Dissolution
Venlafaxine Hydrochloride, Extended Release Capsules, 150 mg, UD-100 Tablets per Box (10 x 10), Rx Only, Manufactured by: Teva Pharmaceuticals USA…
Why was Venlafaxine Hydrochloride recalled?
Failed Dissolution Specification: Out of Specification dissolution results at 12 month interval.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 91357
- Product
- Venlafaxine Hydrochloride, Extended Release Capsules, 150 mg, UD-100 Tablets per Box (10 x 10), Rx Only, Manufactured by: Teva Pharmaceuticals USA…
- Recalling firm
- McKesson Packaging Services
- Quantity
- 1,557 Boxes
- Distribution
- Nationwide
- Recall date
- March 26, 2014
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)