Plastikon Healthcare recalls 100mg-10mg/5mL cough syrup cups due to manufacturing process deviations. Products may not meet quality standards. Consumers should check NDC codes and expiration dates for affected lots.
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Plastikon Healthcare is recalling cough syrup cups that may have been made under uncontrolled manufacturing conditions. This recall is for institutional use products that could potentially not meet quality standards.
The products were manufactured under conditions that did not meet controlled quality standards. This CGMP deviation could mean the product does not meet the required safety and quality levels for institutional use.
Institutional users who purchased the cough syrup cups with NDC codes listed in the recall. The most at-risk individuals are those using the product for medical purposes without proper quality assurance.
Check for NDC codes 0904-6844-70 through 22016A on the packaging. Products with expiration dates from September 2022 through March 2024 are affected.
Verify the NDC code and expiration date on the packaging to confirm if the product is in the recall list.
The recall states there were manufacturing process deviations, but does not specify if the product is unsafe. Consumers should check the recall list to confirm if their specific product is affected.
The recall does not provide a specific remedy, so consumers should check the NDC codes and expiration dates to determine if their product is affected.
Check the NDC codes listed in the recall (0904-6844-70 through 22016A) and expiration dates from September 2022 through March 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-1490-2022 — Plastikon Healthcare Plastikon Healthcare Hello, I own a Plastikon Healthcare that is covered by recall D-1490-2022 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.
