SpecGx recalls 100-tablet prescription oxycodone/acetaminophen tablets due to potential missing imprints. Consumers should check labels for NDC 0406-0522-01 and lot numbers ending in 0522J23493.
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
SpecGx is recalling prescription oxycodone and acetaminophen tablets that may have missing imprints. This could lead to incorrect dosing if the tablet is not properly identified.
The tablets may have missing imprints, which could cause confusion about the medication's identity. This might lead to incorrect dosing if the tablet is not properly identified by the patient.
Prescription holders of the 100-tablet oxycodone/acetaminophen combination. Patients who have the specific NDC 0406-0522-01 lot numbers ending in 0522J23493 are most at risk.
Check for the NDC code 0406-0522-01 on the label. Look for lot numbers ending in 0522J23493 and expiration date 03/2027.
Look for the NDC code 0406-0522-01 and lot number ending in 0522J23493 on the tablet packaging.
The recall is due to a potential missing imprint on the tablets, which could lead to incorrect identification and dosing.
Check for the NDC code 0406-0522-01 and lot numbers ending in 0522J23493 on the label.
The recall does not specify a remedy, so check with your healthcare provider or pharmacist for guidance.
We’ve drafted a message you can send SpecGx to request your refund or repair — edit it as you like.
Subject: Recall D-0255-2026 — SpecGx SpecGx Hello, I own a SpecGx that is covered by recall D-0255-2026 from SpecGx. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.