Abbott recalls ARCHITECT c4000 Processing Modules with serial numbers C400911 to C403061 (and other models) due to dry natural rubber (latex) subcomponent not being labeled. Consumers should check their device for these serial numbers.
The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).
Abbott is recalling certain ARCHITECT c4000 Processing Modules that contain dry natural rubber (latex) but aren't labeled as such. This means the product may cause allergic reactions in people sensitive to latex. The recall affects specific models with serial numbers listed in the notice.
The devices contain dry natural rubber (latex) but aren't labeled as such. This could cause allergic reactions in people sensitive to latex, especially if the rubber comes into contact with skin.
People who own or use the ARCHITECT c4000 Processing Modules with the listed serial numbers (C400911 to C403061) are affected. Those with latex allergies are at higher risk of allergic reactions.
Check your ARCHITECT c4000 Processing Module for serial numbers starting with C400911 through C403061 (and other listed numbers). The product is designed for automated chemistry tests using photometry and potentiometric technology.
Look for the serial number on your ARCHITECT c4000 Processing Module, which starts with C400911 through C403061 (and other listed numbers).
Abbott is recalling ARCHITECT c4000 Processing Modules that contain dry natural rubber (latex) but aren't labeled as such, which could cause allergic reactions in people sensitive to latex.
Check your device's serial number, which starts with C400911 through C403061 (and other listed numbers).
No action is needed if your device's serial number is not listed in the recall.
We’ve drafted a message you can send Abbott Laboratories to request your refund or repair — edit it as you like.
Subject: Recall Z-0682-2024 — Abbott Laboratories Abbott Laboratories Hello, I own a Abbott Laboratories that is covered by recall Z-0682-2024 from Abbott Laboratories. 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.
