Oxycodone Hydrochloride Tablets recall: Labeling Error
Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles, Rx only, Manufactured for Camber Pharmaceuticals, Inc., Piscataway, NJ, Manufactured…
Why was Oxycodone Hydrochloride Tablets recalled?
Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol
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?
Lot Numbers: 17080591 and 17080619, exp 07/19; 17110907 and 17110908, exp 10/19; and 17120986, exp 11/19
- Product
- Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles, Rx only, Manufactured for Camber Pharmaceuticals, Inc., Piscataway, NJ, Manufactured…
- Recalling firm
- Ascent Pharmaceuticals, Inc.
- Quantity
- 45,875 bottles
- Distribution
- Nationwide
- Recall date
- February 7, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)