Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Oxycodone and Acetaminophen CII Tablets USP Recalled by SpecGx, LLC Due to Failed Tablet/Capsule Specification: There is a potential for...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact SpecGx, LLC directly.
Affected Products
Oxycodone and Acetaminophen CII Tablets USP, 10mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0523-01.
Quantity: 287,988 Bottles.
Why Was This Recalled?
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About SpecGx, LLC
SpecGx, LLC has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report