Inova Diagnostics recalls QUANTA-Lyser 240 IFA lab equipment due to faulty power supply that may cause loss of protective grounding. Affected units have serial number 4314.
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 24:0 IFA lab equipment because its power supply may not be properly grounded, which could lead to electrical hazards. This affects specific units with serial number 4314.
The power supply was manufactured without meeting specifications, which could cause the instrument to lose protective grounding. This might lead to electrical shocks or equipment damage if the device is used improperly.
Lab technicians and medical professionals using the QUANTA-Lyser 240 IFA for clinical testing are most at risk. Affected units have serial number 4314.
Check for the product name 'QUANTA-Lyser 240 IFA' and part number GS0242. Affected units have serial number 4314.
Look for the product name 'QUANTA-Lyser 240 IFA', part number GS0242, and serial number 4314.
The recall states the power supply may not be properly grounded, which could lead to electrical hazards, but the exact risk level is not specified.
Check for the product name 'QUANTA-Lyser 240 IFA', part number GS0242, and serial number 4314.
The recall does not specify any remedy steps, so contact Inova Diagnostics for further instructions.
We’ve drafted a message you can send Inova Diagnostics to request your refund or repair — edit it as you like.
Subject: Recall Z-1221-2018 — Inova Diagnostics Inova Diagnostics Hello, I own a Inova Diagnostics that is covered by recall Z-1221-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
