Plastikon Healthcare recalls acetaminophen oral solution due to manufacturing control deviations. Products may not meet quality standards. Check NDC 0904-6739-71 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 inadequate control. This recall is due to potential quality issues that could affect product safety.
The products were manufactured under conditions that did not meet controlled manufacturing processes. This CGMP deviation could lead to potential quality issues, but the specific risk to consumers is not clearly described in the recall notice.
Institutional users such as hospitals and healthcare facilities that purchased the recalled acetaminophen oral solution. The most at-risk individuals are those using the product without proper quality assurance.
Check for NDC 0904-6739-71 and lot numbers listed in the recall: 20062A, 20067A, 20092A, 20093A, 20101A, 21110A, 20108A, 21012A, 21044A, 21048B, 21053A, 21063B, 21068B, 21084B, 21090A, 21119A, 21122B, 22001B, 22006A, 22017B. Products were sold for institutional use only.
Verify the NDC code 0904-6739-71 and lot numbers listed in the recall notice to determine if your product is affected.
The recall notice states there were manufacturing control deviations, but does not specify if the product is safe to use. Consumers should check the product details to see if it is affected.
The recall notice does not provide a remedy, so affected products should be checked against the listed lot numbers and NDC code to determine if they need to be discarded or returned.
Check the NDC code 0904-6739-71 and lot numbers listed in the recall notice: 20062A, 20067A, 20092A, 20093A, 20101A, 21110A, 20108A, 21012A, 21044A, 21048B, 21053A, 21063B, 21068B, 21084B, 21090A, 21119A, 21122B, 22001B, 22006A, 22017B.
We’ve drafted a message you can send Plastikon Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-1485-2022 — Plastikon Healthcare Plastikon Healthcare Hello, I own a Plastikon Healthcare that is covered by recall D-1485-2022 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.
