Aurobindo Pharma USA Inc recalls Gabapentin Capsules, USP 300 mg, 100-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141; Man…
- Recall date
- October 17, 2014
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0330-2015
- FDA classification
- Class II
- Brand / firm
- Aurobindo Pharma USA Inc
- Sold / distributed
- Nationwide
Why it was recalled
Failed Tablet/Capsule Specifications: Complaints of empty capsules received.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What 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.
Get recall alerts
Free email alert whenever Aurobindo Pharma USA Inc has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Aurobindo Pharma USA Inc