Gabapentin Capsules, USP 300 mg, 100-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141; Manufactured by: Aurobindo Pharma Limited, Unit-VII (SEZ), Mahaboob Nagar (Dt), AP-509302, INDIA, NDC 16714-662-01, UPC 3 16714-662-01 5.
Reported: January 14, 2015 Initiated: October 17, 2014 #D-0330-2015
Product Description
Gabapentin Capsules, USP 300 mg, 100-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141; Manufactured by: Aurobindo Pharma Limited, Unit-VII (SEZ), Mahaboob Nagar (Dt), AP-509302, INDIA, NDC 16714-662-01, UPC 3 16714-662-01 5.
Reason for Recall
Failed Tablet/Capsule Specifications: Complaints of empty capsules received.
Details
- Recalling Firm
- Aurobindo Pharma USA Inc
- Units Affected
- 24,816 bottles
- Distribution
- Nationwide
- Location
- Dayton, NJ
Frequently Asked Questions
What product was recalled? ▼
Gabapentin Capsules, USP 300 mg, 100-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141; Manufactured by: Aurobindo Pharma Limited, Unit-VII (SEZ), Mahaboob Nagar (Dt), AP-509302, INDIA, NDC 16714-662-01, UPC 3 16714-662-01 5.. Recalled by Aurobindo Pharma USA Inc. Units affected: 24,816 bottles.
Why was this product recalled? ▼
Failed Tablet/Capsule Specifications: Complaints of empty capsules received.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 14, 2015. Severity: Moderate. Recall number: D-0330-2015.
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