Plastikon Healthcare recalls acetaminophen oral solution due to failed microbial testing. Products distributed for institutional use only may have contamination risks.
CGMP Deviations: Failure to properly investigate failed microbial testing.
Plastikon Healthcare is recalling acetaminophen oral solution for institutional use because of microbial testing failures. This could pose a contamination risk to users.
The product failed microbial testing, indicating potential contamination. This could lead to health risks if the solution is consumed by users.
Institutional users, such as hospitals or clinics, may be affected. Individuals using this product for medical purposes should check if they have the recalled items.
Look for the product labeled 'Acetaminophen Oral Solution, USP 650mg/ 20.3 mL cup' in 10-cup trays, 10 trays per carton. The lot number 20040A with expiration May 2022 is associated with this recall.
Verify the lot number and expiration date on the product packaging to determine if it is recalled.
The recall indicates potential contamination risks due to failed microbial testing, so it is not recommended for use until the recall is addressed.
Check the lot number and expiration date. If it matches the recalled items (lot 20040A, exp May 2022), contact Plastikon Healthcare for guidance.
Look for the product description and lot number 20040A with expiration May 2022 on the packaging.
We’ve drafted a message you can send Plastikon Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0869-2022 — Plastikon Healthcare Plastikon Healthcare Hello, I own a Plastikon Healthcare that is covered by recall D-0869-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.