Abbott recalls two blood analyzers due to unlabeled natural rubber latex in components. Affected models include CD-Ruby and CD Sapphire with specific serial numbers. Consumers should check their devices for latex content.
The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).
Abbott is recalling two blood analyzers, the CELL-DYN Ruby and Sapphire models, because they contain natural rubber latex that isn't labeled as such. This could cause allergic reactions in sensitive individuals who are allergic to latex.
The devices contain natural rubber latex that isn't clearly labeled. This could cause allergic reactions in people sensitive to latex, though the risk is low for most users.
People who own or use these blood analyzers are affected. Those with latex allergies are at higher risk of reactions.
Check for the model names: CELL-DYN Ruby (CD-Ruby) or CELL-DYN Sapphire (CD Sapphire). The specific serial numbers are listed in the recall notice.
Look for the model name on your device: CELL-DYN Ruby (CD-Ruby) or CELL-DYN Sapphire (CD Sapphire).
Yes, they contain natural rubber latex that isn't labeled as such.
Check your device model and serial number to see if it's affected. The recall includes specific models and serial numbers.
The risk is low for most users, but people with latex allergies could have reactions.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-0604-2024 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-0604-2024 from Abbott. 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.
