Microtek Medical recalls Ecolab medical bags and drapes with naphthalene odor. Affected lots have potential health risks from strong chemical smell. Consumers should check product details and contact Microtek for remedy.
Certain lots of the products have a Naphthalene odor.
Microtek Medical is recalling specific Ecolab medical bags and drapes due to a naphthalene odor in certain lots. This odor could cause health issues for people sensitive to strong chemical smells, especially in healthcare settings where these products are used.
Naphthalene is a chemical found in mothballs and some industrial products. The odor in these recalled items could irritate the respiratory system or cause discomfort for individuals sensitive to strong smells, particularly in enclosed medical environments.
Healthcare workers and patients using these medical drapes and bags in hospitals or clinics are most at risk. People with heightened sensitivity to chemical odors may experience discomfort or health effects.
Check for the model numbers and lot numbers listed in the recall notice: Model 63620RT (Lot 220301F), Model 60040S (Lot 220305F), Model 60050S (Lot 220305F), Model 890017 (Lots 220110F, 220108F, 220102F, 211231F), and Model 4951N (Lots 220110F, 220109F).
Review the model numbers and lot numbers listed in the recall notice to confirm if your item is affected.
The recall is for certain lots of Ecolab medical bags and drapes that have a naphthalene odor, which could cause respiratory irritation or discomfort for sensitive individuals.
Check the model number and lot number on your product. Affected items include specific models with the lot numbers listed in the recall notice.
The recall notice does not specify a remedy, so contact Microtek Medical directly for further instructions.
We’ve drafted a message you can send Ecolab to request your refund or repair — edit it as you like.
Subject: Recall Z-2250-2023 — Ecolab Ecolab Hello, I own a Ecolab that is covered by recall Z-2250-2023 from Ecolab. 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.
