FDA recall record

Oxycodone and Acetaminophen CII Tablets USP, 7.5 mg/325 mg, 100 tablets recall — FDA D-0255-2026

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

Class IIclassification
D-0255-2026official record ID
Jan 14, 2026report date

Recall record at a glance

Official recordD-0255-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmSpecGx, LLC
Report dateJan 14, 2026
Recall initiation dateDec 16, 2025
Quantity74,544 bottles
LocationWebster Groves, MO, United States

Official product description

Oxycodone and Acetaminophen CII Tablets USP, 7.5 mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0522-01. Case label: SpecGx LLC, NDC 0406052201, Exp. 2027/03, Lot: 0522J23493

Why the product was recalled

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

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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