PerkinElmer recalls QSight 210 MD mass spectrometers with Hot Fix 2 software that may overwrite last sample data when automatic flush is enabled. Affected units have specific part numbers.
Under certain conditions when using PerkinElmer QSight 210 MD mass spectrometer with Simplicity 3Q MD and Hotfix 2 software, it is possible for the original data from the last acquired sample to be over-written when the automatic flush is enabled.
PerkinElmer is recalling mass spectrometers that could overwrite the last sample's data when automatic flush is enabled in specific software versions. This could lead to inaccurate test results if the data is overwritten.
The software may overwrite the original data from the last acquired sample when automatic flush is enabled. This could cause inaccurate test results if the data is overwritten without proper verification.
Users of PerkinElmer QSight 210 MD mass spectrometers with Simplicity 3Q MD software and Hot Fix 2 software version 1.0 are affected. Laboratory technicians and researchers using these devices for sample analysis are most at risk.
Check for part numbers: 210MDBC709100008, 210MD8C709140010, 210MD8C709150009, and other listed numbers. The device includes Simplicity 3Q MD software and Hot Fix 2 software version 1.0.
Verify if your device has Simplicity 3Q MD software and Hot Fix 2 software version 1.0.
The original data from the last acquired sample could be overwritten, potentially causing inaccurate test results.
Check for part numbers listed in the recall: 210MDBC709100008, 210MD8C709140010, 210MD8C709150009, and other specific numbers.
No, the recall does not require stopping use. Users should check software version and ensure data is verified before proceeding.
We’ve drafted a message you can send PerkinElmer to request your refund or repair — edit it as you like.
Subject: Recall Z-0513-2019 — PerkinElmer PerkinElmer Hello, I own a PerkinElmer that is covered by recall Z-0513-2019 from PerkinElmer. 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.
