Madison Polymeric Engineering recalls Draco Enzymatic Deep-Cleaning Pads (Product Number HY0305Z) due to contamination with Pseudomonas bacteria. Affected lots EX20190419P through EX20190424P were sold for use on medical instruments.
The product is contaminated with Pseudomonas.
Madison Polymeric Engineering is recalling Draco Enzymatic Deep-Cleaning Pads (Product Number HY0305Z) because they contain Pseudomonas bacteria. This contamination could pose a health risk if the pads are used on medical instruments, potentially leading to infections.
The pads contain Pseudomonas bacteria, which can cause infections if medical instruments are not properly sterilized after cleaning. Pseudomonas is a type of bacteria that can lead to serious infections in healthcare settings.
Medical professionals and facilities using the Draco Enzymatic Deep-Cleaning Pads for surgical instruments or endoscopes are most at risk. The recall affects specific lot numbers produced in April 2019.
Check for the product number HY0305Z on the pads. Affected lots are EX20190419P, EX20190420P, EX20190423P, and EX20190424P, produced in April 2019.
Look for the lot numbers EX20190419P, EX20190420P, EX20190423P, or EX20190424P on the pads.
The pads are contaminated with Pseudomonas bacteria and should not be used on medical instruments. They are not safe for use in healthcare settings.
Check the lot number on the pads. If it matches EX20190419P, EX20190420P, EX20190423P, or EX20190424P, stop using them and contact Madison Polymeric Engineering for instructions.
The recall does not provide a fix; affected pads should be discarded or returned to the manufacturer.
We’ve drafted a message you can send Madison Polymeric Engineering to request your refund or repair — edit it as you like.
Subject: Recall Z-0969-2019 — Madison Polymeric Engineering Madison Polymeric Engineering Hello, I own a Madison Polymeric Engineering that is covered by recall Z-0969-2019 from Madison Polymeric Engineering. 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.