Venlafaxine Hydrochloride extended release capsules recall
Venlafaxine Hydrochloride extended release capsules, 37.5 mg, 30-count bottles, Rx Only, Manufactured for: Aurobindo Pharma USA, Inc. 2400 Route 130…
Why was Venlafaxine Hydrochloride extended release capsules recalled?
Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or clumped/melted capsules.
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 #: VI3716010-A, Exp. 04/2018
- Product
- Venlafaxine Hydrochloride extended release capsules, 37.5 mg, 30-count bottles, Rx Only, Manufactured for: Aurobindo Pharma USA, Inc. 2400 Route 130…
- Recalling firm
- Aurobindo Pharma USA Inc
- Quantity
- 47,040 bottles
- Distribution
- Nationwide in the US
- Recall date
- February 22, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)