RecallRadar

FDA Drug recall D-0254-2026

Oxycodone and Acetaminophen CII Tablets USP, 10mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0523-01

On 2026-01-14 the FDA classified a Class II recall of Oxycodone and Acetaminophen CII Tablets USP, 10mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0523-01 by Specgx, citing failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0254-2026
ClassificationClass II
Statusongoing
Initiated2025-12-16
Published2026-01-14
Last updated2026-09-13 11:52 UTC
CompanySpecgx
DistributionUS

Product

Oxycodone and Acetaminophen CII Tablets USP, 10mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0523-01.

Reason

Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.

Identifiers

ndc0406-0512-01
ndc0406-0512-05
ndc0406-0512-62
ndc0406-0512-23
ndc0406-0512-91
ndc0406-0522-01
ndc0406-0522-62
ndc0406-0522-05
ndc0406-0522-23
ndc0406-0523-01
ndc0406-0523-62
ndc0406-0523-05
ndc0406-0523-23
code_infoLot: 0523J23904, expires: 05/2027; 0523J24426, 0523J24427, expires: 06/2027.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0254-2026%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.