Plastikon Healthcare recalls acetaminophen oral solution due to manufacturing process deviations. Products may not meet quality standards. Check NDC 0904-6820-76 and lot numbers for affected items.
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Plastikon Healthcare is recalling acetaminophen oral solution products that were manufactured under conditions with uncontrolled processes. This recall is due to potential quality issues that could affect product safety.
The products were made under manufacturing conditions that did not meet controlled quality standards. This CGMP deviation could lead to inconsistent product quality, but the recall does not specify a direct health risk or injury mechanism.
Institutional users who purchased the acetaminophen oral solution with NDC 0904-6820-76 and specific lot numbers listed in the recall. Healthcare facilities and institutions using this product are most at risk.
Check for the NDC code 0904-6820-76 on the product packaging. Look for specific lot numbers listed in the recall, such as 20064A, 20066A, and others with expiration dates through January 2024.
Identify the NDC code 0904-6820-76 and lot numbers from the recall list to confirm if your product is affected.
The recall does not indicate a specific health risk or injury mechanism. The products were manufactured under uncontrolled conditions, but no immediate danger is stated.
The recall does not provide a remedy or action steps. Check the product details to see if it matches the listed NDC and lot numbers.
Look for the NDC code 0904-6820-76 and specific lot numbers listed in the recall, such as 20064A, 20066A, and others with expiration dates through January 2024.
We’ve drafted a message you can send Plastikon Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-1486-2022 — Plastikon Healthcare Plastikon Healthcare Hello, I own a Plastikon Healthcare that is covered by recall D-1486-2022 from Plastikon Healthcare. 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.
