RecallRadar

FDA Drug recall D-1150-2015

OXYCODONE HCl C-II Tablets, 5 mg USP, 100-count blister cards, Rx only, Manufactured by Nesher Pharmaceuticals USA LLC., St. Louis, MO 6304…

On 2015-07-08 the FDA classified a Class II recall of OXYCODONE HCl C-II Tablets, 5 mg USP, 100-count blister cards, Rx only, Manufactured by Nesher Pharmaceuticals USA LLC., St. Louis, MO 6304… by The Harvard Drug Group, citing superpotent Drug: Confirmed customer complaint of a single unit dose blister cavity containing 2 OXYCODONE HCl 5 mg tablets.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1150-2015
ClassificationClass II
Statusterminated
Initiated2015-06-10
Published2015-07-08
Last updated2026-09-13 11:51 UTC
CompanyThe Harvard Drug Group
DistributionUS

Product

OXYCODONE HCl C-II Tablets, 5 mg USP, 100-count blister cards, Rx only, Manufactured by Nesher Pharmaceuticals USA LLC., St. Louis, MO 63044, Distributed by Major Pharmaceuticals, Livonia, MI 48150, NDC 0904-6444-61.

Reason

Superpotent Drug: Confirmed customer complaint of a single unit dose blister cavity containing 2 OXYCODONE HCl 5 mg tablets.

Identifiers

code_infoLot # P-20000; Exp. 08/16 Lot # P-20004; Exp. 08/16

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1150-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.