Prednisone Tablet USP recall: Labeling Error
Prednisone Tablet USP, 20 mg tablets, packaged in blisters of ten (10) tablets per blister card, ten blister cards per carton, Roxanne, Columbus, OH --- NDC 0054-0018-20
Why was Prednisone Tablet USP recalled?
Labeling: Missing Label; missing label on blister card
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
The affected product consists of lot #261739A, expiration date OCT 2014.
- Product
- Prednisone Tablet USP, 20 mg tablets, packaged in blisters of ten (10) tablets per blister card, ten blister cards per carton, Roxanne, Columbus, OH --- NDC 0054-0018-20
- Recalling firm
- Boehringer Ingelheim Roxane Inc
- Quantity
- 14,619 cartons
- Distribution
- Nationwide
- Recall date
- August 21, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)