Reported Jan 29, 2014 · Terminated
PREGABALIN, Capsule, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00071101768.
Aidapak Services, LLC
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: Aidapak Services, LLC · 14301 Se 1st St · Vancouver, WA · 98684-3501
Is this the product you have?
- PREGABALIN, Capsule, 200 mg, Rx only
- Distributed byAidaPak Service, LLC, NDC 00071101768
- Lot codes and dates
6 of 6 products
Products covered by this recall # Product as published 1 Label Mixup: PREGABALIN, Capsule, 200 mg has the following codes: Pedigree: AD21787_1, EXP: 5/1/2014 2 Pedigree: AD30024_1, EXP: 5/9/2014 3 Pedigree: AD73518_4, EXP: 5/31/2014 4 Pedigree W002759, EXP: 6/6/2014 5 Pedigree: W003397, EXP: 6/19/2014 6 Pedigree: W003398, EXP: 6/19/2014. - Amount recalled
- 540 Capsules
This recall covers 265 products
The agency filed one notice per product. You are reading one of them; the other 264 are below.
252 more are in the archive.
Where it was sold
Why it was recalled
Labeling: Label Mixup: PREGABALIN, Capsule, 200 mg may have potentially been mislabeled as one of the following drugs: LOSARTAN POTASSIUM, Tablet, 50 mg, NDC 00781570192, Pedigree: AD21965_10, EXP: 5/1/2014; CYANOCOBALAMIN, Tablet, 500 mcg, NDC 00536355101, Pedigree: AD30180_25, EXP: 5/9/2014; clonazePAM, Tablet, 0.25 mg (1/2 of 0.5 mg), NDC 00093083201, Pedigree: AD73518_1, EXP: 5/31/2014; OM
This product could cause temporary or reversible health problems — stop using it.
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