Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, 90 capsules per bottle, Rx Only, GSMS, NDC # 60429-122-90
Reported: August 24, 2016 Initiated: August 3, 2016 #D-1459-2016
Product Description
Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, 90 capsules per bottle, Rx Only, GSMS, NDC # 60429-122-90
Reason for Recall
Failed Dissolution Specifications: Out-of-specification results in retained sample.
Details
- Recalling Firm
- Golden State Medical Supply Inc.
- Units Affected
- 40,631 bottles
- Distribution
- Nationwide
- Location
- Camarillo, CA
Frequently Asked Questions
What product was recalled? ▼
Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, 90 capsules per bottle, Rx Only, GSMS, NDC # 60429-122-90. Recalled by Golden State Medical Supply Inc.. Units affected: 40,631 bottles.
Why was this product recalled? ▼
Failed Dissolution Specifications: Out-of-specification results in retained sample.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 24, 2016. Severity: Moderate. Recall number: D-1459-2016.
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