Ameditech recalls Oratect III oral fluid drug screening devices due to potential false positive results. Affected units include all lots within expiry date. Consumers should contact Ameditech for details.
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Ameditech is recalling its Orate:ct III oral fluid drug screen devices because they may give false positive results. This could lead to incorrect drug test outcomes, which might affect legal or medical decisions.
The device may produce false positive results, meaning it could indicate the presence of drugs when none are actually present. This can lead to incorrect conclusions in drug testing scenarios.
People who own or use the Oratect III oral fluid drug screening device are affected. Those who have used the device for drug testing are most at risk of receiving inaccurate results.
Check for the model number HM12-CE on the device. The recall includes all lots of the Oratect III device within its expiry date.
Reach out to Ameditech directly for specific instructions on how to handle the device.
The recall is due to potential false positive results in drug testing, which could lead to incorrect outcomes.
The affected model is HM12-CE for the Oratect III Oral Fluid Drug Screen Device.
No, the recall does not require immediate discontinuation; contact Ameditech for specific instructions.
We’ve drafted a message you can send Ameditech to request your refund or repair — edit it as you like.
Subject: Recall Z-3041-2020 — Ameditech Ameditech Hello, I own a Ameditech that is covered by recall Z-3041-2020 from Ameditech. 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.
