Recall D-0255-2026

US Class II Ongoing · initiated 2025-12-16

Recalling firm

SpecGx, LLC, MO

Product

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

Reason for recall

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

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