Zyla Life Sciences recalls 7.5mg Oxaydo tablets due to lower potency than labeled. Affected products have NDC 69344-213-11, Lot 22W02, expiring 01/31/2025. No remedy specified in recall.
Sub-potent Drug: Lower potency than labeled.
Zyla Life Sciences is recalling 7.5mg Oxaydo (oxycodone) tablets because they contain less active ingredient than labeled. This means the medication may not work as intended for pain relief. The recall affects prescription bottles with specific NDC and lot numbers.
The tablets have lower potency than labeled, meaning they contain less active oxycodone per dose than advertised. This could result in the medication not providing the intended pain relief. The risk is primarily for patients who rely on the medication for pain management.
Prescription holders of Oxaydo 7.5mg tablets with NDC 69344-213-11 and Lot 22W02. Patients taking this medication for pain relief are most at risk of inadequate pain control.
Check for the NDC code 69344-213-11 and lot number 22W02 on the bottle. The product expires January 31, 2025. This is a prescription-only medication.
Verify the NDC code 69344-213-11 and lot number 22W02 on the bottle label.
The recall record does not specify any remedy.
The recalled product expires January 31, 2025.
Look for the NDC code 69344-213-11 and lot number 22W02 on the bottle label.
We’ve drafted a message you can send Zyla Life Sciences to request your refund or repair — edit it as you like.
Subject: Recall D-0094-2024 — Zyla Life Sciences Zyla Life Sciences Hello, I own a Zyla Life Sciences that is covered by recall D-0094-2024 from Zyla Life Sciences. 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.
