Reported Feb 22, 2017 · Terminated
Venlafaxine Hydrochloride extended release capsules, 37.5 mg, 30-count bottles, Rx Only, Manufactured for: Aurobindo…
Aurobindo Pharma USA Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Aurobindo Pharma USA Inc · 666 Plainsboro Rd Ste 210 · Plainsboro, NJ · 08536-3004
Is this the product you have?
- Venlafaxine Hydrochloride extended release capsules, 37.5 mg, 30-count bottles, Rx Only
- Manufactured forAurobindo Pharma USA, Inc. 2400 Route 130 North, Dayton
- NJ 08810 Manufactured byAurobindo Pharma Limited Hyderabad-500 072 India, NDC 65862-527-30
- Lot codes and dates
Lot #: VI3716010-AExp. 04/2018
- Amount recalled
- 47,040 bottles
Where it was sold
- Nationwide
Why it was recalled
Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or clumped/melted capsules.
This product could cause temporary or reversible health problems — stop using it.
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