Inova Diagnostics recalls QUANTA-Lyser 240 EIA (Part #GS0241) due to faulty power supply causing loss of protective grounding. Affected units may have electrical damage risks.
The device power supply was not manufactured according to specification which can result in the loss of the protective grounding of the instrument.
Inova Diagnostics is recalling the QUANTA-Lyser 240 EIA instrument because its power supply was made incorrectly, which could cause the protective grounding to fail. This means the device might not have proper electrical safety, potentially leading to electrical damage or injury if used improperly.
The power supply was manufactured without meeting specifications, which can cause the protective grounding to fail. This means the device might not have proper electrical safety, potentially leading to electrical damage or injury if used improperly.
Users of the QUANTA-Lyser 240 EIA instrument for clinical testing are affected. Laboratory technicians and medical staff who use this device are most at risk.
Check for the model name QUANTA-Lyser 240 EIA and part number GS0241. The instrument has a serial number 4316.
Identify the model name QUANTA-Lyser 240 EIA and part number GS0241 to confirm if your device is affected.
The recall states the power supply issue could cause loss of protective grounding, but the record does not specify if this leads to injury or damage in normal use.
The recall record does not provide specific action steps for affected users.
Check for the model name QUANTA-Lyser 240 EIA and part number GS0241. The instrument has a serial number 4316.
We’ve drafted a message you can send Inova Diagnostics to request your refund or repair — edit it as you like.
Subject: Recall Z-1222-2018 — Inova Diagnostics Inova Diagnostics Hello, I own a Inova Diagnostics that is covered by recall Z-1222-2018 from Inova Diagnostics. 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.
