FDA Drug recall D-0248-2018
Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles, Rx only, Manufactured for Camber Pharmaceuticals, Inc., Piscataway, NJ, Manu…
- FDA Drug
- Class III
- terminated
- Published 2018-02-07
On 2018-02-07 the FDA classified a Class III recall of Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles, Rx only, Manufactured for Camber Pharmaceuticals, Inc., Piscataway, NJ, Manu… by Ascent Pharmaceuticals, citing labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0248-2018 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2018-01-22 |
| Published | 2018-02-07 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Ascent Pharmaceuticals |
| Distribution | US |
Product
Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles, Rx only, Manufactured for Camber Pharmaceuticals, Inc., Piscataway, NJ, Manufactured by: Ascent Pharmaceuticals, Inc., Central Islip, NY --- NDC 31722-917-01
Reason
Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol
Identifiers
| ndc | 31722-484-01 |
|---|---|
| ndc | 31722-484-05 |
| ndc | 31722-485-01 |
| ndc | 31722-485-05 |
| ndc | 31722-917-01 |
| ndc | 31722-917-05 |
| ndc | 31722-486-01 |
| ndc | 31722-486-05 |
| ndc | 31722-918-01 |
| ndc | 31722-918-05 |
| code_info | Lot Numbers: 17080591 and 17080619, exp 07/19; 17110907 and 17110908, exp 10/19; and 17120986, exp 11/19 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0248-2018%22
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