Drug recall D-0255-2026
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.
Lots and codes
Lot: 0522J23493, expires: 03/2027.
Recall details
- Recalling firm
- SpecGx, LLC, Webster Groves, MO
- Quantity
- 74,544 bottles
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- December 16, 2025
Related products
- Oxycodone And Acetaminophen – drug information
- NDC 0406-0512 Oxycodone And Acetaminophen · Oxycodone Hydrochloride 5 mg/1; Acetaminophen 325 mg/1 · SpecGx LLC
- NDC 0406-0523 Oxycodone And Acetaminophen · Oxycodone Hydrochloride 10 mg/1; Acetaminophen 325 mg/1 · SpecGx LLC
- NDC 0406-0522 Oxycodone And Acetaminophen · Oxycodone Hydrochloride 7.5 mg/1; Acetaminophen 325 mg/1 · SpecGx LLC