Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

PerkinElmer 226 Sample Collection Device Recalled by PerkinElmer Health Sciences, Inc. Due to PerkinElmer 226 Sample Collection Devices Lot Number 40020001...

Date: December 19, 2017
Company: PerkinElmer Health Sciences, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact PerkinElmer Health Sciences, Inc. directly.

Affected Products

PerkinElmer 226 Sample Collection Device

Quantity: 164,952 devices

Why Was This Recalled?

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.

Where Was This Sold?

US distribution in the state of Ohio

About PerkinElmer Health Sciences, Inc.

PerkinElmer Health Sciences, Inc. has 10 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report