PerkinElmer recalls 226 Sample Collection Devices with serial numbers that don't match pack labels. Affected units have specific serial ranges and lot numbers. Consumers should check their device details.
PerkinElmer 226 Sample Collection Devices Lot Number 40020001 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained within the pack.
PerkinElmer is recalling certain 226 Sample Collection Devices because the serial numbers on the device packages don't match the actual serial numbers of the devices inside. This mismatch could lead to confusion when trying to verify the device's authenticity or compliance.
The serial numbers printed on the device packaging do not match the serial numbers of the devices inside the pack. This mismatch could cause confusion when verifying the device's authenticity or compliance with regulatory standards.
Users of PerkinElmer 226 Sample Collection Devices with specific serial numbers (06879601-06879700) and lot number 40020001 are affected. Healthcare professionals and lab personnel using these devices are most at risk.
Check if your PerkinElmer 226 Sample Collection Device has a serial number between 06879601 and 06879700 and lot number 40020001. The device packaging should show the lot number and serial number range as listed in the recall notice.
Verify your PerkinElmer 226 Sample Collection Device's serial number and lot number against the specified range (06879601-06879700) and lot number 40020001.
The affected devices have serial numbers from 06879601 to 06879700.
The affected devices have lot number 40020001.
No, the recall does not require immediate discontinuation. You can continue using the device but should verify the serial number and lot number.
We’ve drafted a message you can send PerkinEl:mer to request your refund or repair — edit it as you like.
Subject: Recall Z-2264-2020 — PerkinEl:mer PerkinEl:mer Hello, I own a PerkinEl:mer that is covered by recall Z-2264-2020 from PerkinEl:mer. 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.
