Omeza recalls 10 vials of lidocaine lavage pain relief oil due to CGMP deviations. Affected lots expire 04/24/2024 or 01/25/2024. No specific remedy stated in recall notice.
CGMP Deviations
Omeza is recalling 10 vials of lidocaine lavage pain relief oil that were manufactured with CGMP deviations. This means the product may not meet safety standards, though the exact risk isn't specified in the recall notice.
CGMP deviations refer to failures in manufacturing quality control processes. This could mean the product doesn't meet safety standards, but the recall notice doesn't specify the exact hazard or how serious it is.
People who own or use Omeza Lidocaine Lavage pain relief oil vials with the specified lot numbers and expiration dates are affected. Those using the product for pain relief are most at risk if the product is unsafe.
Check the lot number on the vial: 28622 2-1 or 286222-3. The expiration dates are either 04/24/2024 or 01/25/2024 (or 04/25/2024).
Look for the lot number (28622 2-1 or 286222-3) and expiration date on the vial.
The recall notice does not state any remedy or action steps.
The recall mentions CGMP deviations, which are manufacturing quality control failures, but does not specify the exact hazard or risk level.
Check the lot number (28622 2-1 or 286222-3) and expiration date (04/24/2024 or 01/25/2024 or 04/25/2024).
We’ve drafted a message you can send Omeza to request your refund or repair — edit it as you like.
Subject: Recall D-0288-2024 — Omeza Omeza Hello, I own a Omeza that is covered by recall D-0288-2024 from Omeza. 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.
