Madison Polymeric Engineering recalls First Step Draco Pad (EP-4D) due to contamination with Stenotrophomonas lactiubi. Affected units include specific lot numbers from December 2019.
This product has been contaminated with Stenotrophomonas lactiubi.
Madison Polymeric Engineering is recalling First Step Draco Pads with product number EP-4D because they were contaminated with Stenotrophomonas lactiubi. This contamination could pose a health risk if the pads are used without proper cleaning.
The pads were contaminated with Stenotrophomonas lactiubi, a type of bacteria that can cause infections if not properly cleaned. This contamination occurs during manufacturing and may not be visible to the user.
Users of First Step Draco Pads with product number EP-4D and specific lot numbers from December 2019 are affected. Those with the contaminated pads are at risk of potential health issues.
Check for product number EP-4D on the pad. Affected units include lot numbers EX20191221X, EX20191226X, EX20191227X, and EX20191228X from December 2019.
Look for product number EP-4D and lot numbers EX20191221X, EX20191226X, EX20191227X, or EX20191228X on the pad.
The recall record states the product was contaminated with Stenotrophomonas lactiubi, but does not specify the exact health risks.
Check for product number EP-4D and lot numbers EX20191221X, EX20191226X, EX20191227X, or EX20191228X.
The recall record does not specify a remedy, so the official notice does not state what action to take.
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-1925-2019 — Madison Polymeric Engineering Madison Polymeric Engineering Hello, I own a Madison Polymeric Engineering that is covered by recall Z-1925-2019 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.