Lyrica (pregabalin) capsules, 50 mg, 90-count bottle, Rx only, Distributed by: Parke-Davis, Division of Pfizer Inc., NY, NY 10017, NDC 0071-1013-68
Reported: February 10, 2016 Initiated: January 11, 2016 #D-0648-2016
Product Description
Lyrica (pregabalin) capsules, 50 mg, 90-count bottle, Rx only, Distributed by: Parke-Davis, Division of Pfizer Inc., NY, NY 10017, NDC 0071-1013-68
Reason for Recall
FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of pregabalin capsules due to the potential presence of deformed or damaged capsules.
Details
- Recalling Firm
- Pfizer Inc.
- Units Affected
- 30,672 bottles
- Distribution
- Nationwide and Puerto Rico
- Location
- New York, NY
Frequently Asked Questions
What product was recalled? ▼
Lyrica (pregabalin) capsules, 50 mg, 90-count bottle, Rx only, Distributed by: Parke-Davis, Division of Pfizer Inc., NY, NY 10017, NDC 0071-1013-68. Recalled by Pfizer Inc.. Units affected: 30,672 bottles.
Why was this product recalled? ▼
FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of pregabalin capsules due to the potential presence of deformed or damaged capsules.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 10, 2016. Severity: Moderate. Recall number: D-0648-2016.
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