Quest International recalls measles IgM test kits without premarket approval. These kits may not be safe for use. Affected models include 01-190M with lots G00024, K040:12024, etc.
Measles IgM Test Kit lacks premarket approval or clearance.
Quest International recalls measles IgM test kits that lack premarket approval. This means the test kits may not be safe for use and could pose health risks if used improperly.
The test kits lack premarket approval or clearance, meaning they haven't been reviewed by the FDA for safety and effectiveness. This could lead to inaccurate results or potential health risks if used without proper oversight.
People who own or use the Quest Measles IgM test kits with model 01-190M and affected lots (G00024, K04024, M11024, M12024, D01025, E04025, F04025) are affected. Healthcare providers and individuals testing for measles may be at risk.
Check the model number on the kit, which is 01-190M. Look for affected lots: G00024, K04024, M11024, M12024, D01025, E04025, or F04025.
Look for the model number 01-190M on the kit.
Check if your kit has one of the affected lots: G00024, K04024, M11024, M12024, D01025, E04025, or F04025.
The test kit lacks premarket approval or clearance, meaning it hasn't been reviewed by the FDA for safety and effectiveness.
The affected model number is 01-190M.
The affected lots are G00024, K04024, M11024, M12024, D01025, E04025, and F04025.
We’ve drafted a message you can send Quest to request your refund or repair — edit it as you like.
Subject: Recall Z-2552-2025 — Quest Quest Hello, I own a Quest that is covered by recall Z-2552-2025 from Quest. 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.
