Hudson Scientific recalls iTOVi Tracker/Scanner models ITS10 and ITS15 due to electric shocks from improper manufacturing. Affected units have specific lot and serial numbers. Stop using immediately to avoid injury.
The device and its accessories may not have been manufactured according to current Good Manufacturing Practices. In addition, the firm has received three complaints regarding electric shocks received when using the device.
Hudson Scientific is recalling iTOVi Tracker/Scanner models ITS10 and ITS15 because they may not have been made properly, leading to electric shocks. This could cause injury if used without proper safety checks.
The device may not have been manufactured correctly, which can cause electric shocks when in use. Three complaints have been reported about receiving electric shocks from these devices.
Users of the iTOVi Tracker/Scanner models ITS10 and ITS15 who purchased the device between 2016 and 2018 are affected. People using the device for health monitoring are most at risk due to potential electric shocks.
Check for model numbers ITS10 or ITS15 on the device. Look for lot numbers from 012016 to 092017 and serial numbers starting with 35,949.
The device may cause electric shocks, so stop using it right away to avoid injury.
Hudson Scientific received three complaints about electric shocks from the device, and it may not have been manufactured according to current Good Manufacturing Practices.
The affected models are ITS10 and ITS15.
Check the device for model numbers ITS10 or ITS15, and look for lot numbers from 012016 to 092017 and serial numbers starting with 35,949.
We’ve drafted a message you can send Hudson Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-2736-2018 — Hudson Scientific Hudson Scientific Hello, I own a Hudson Scientific that is covered by recall Z-2736-2018 from Hudson Scientific. 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.
