Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
DELFIA¿ PC with V3.0 Software Recalled by PerkinElmer Health Sciences, Inc. Due to AutoDELFIA System with Version 3.0 Software: Potential plate...
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
DELFIA¿ PC with V3.0 Software, Fluorometer, for clinical use Product Number: 1235-8100 Product Usage: The Wallac 1235 AutoDELFIA automatic immunoassay system is designed to automatically perform assays using the DELFIA technology. DELFIA technology is based on the proven and widely used method of time resolved fluorometry
Quantity: 1 US ; 3 OUS
Why Was This Recalled?
AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About PerkinElmer Health Sciences, Inc.
PerkinElmer Health Sciences, Inc. has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report