PerkinElmer Health Sciences, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1101-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Program Update Package AutoDELFIA¿ 3.0, Fluorometer, for clinical use Product Number: 1235-8110 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

Product Classification:

Class III

Date Initiated: December 21, 2016

Date Posted: February 1, 2017

Recall Number: Z-1101-2017

Event ID: 75949

Reason for Recall:

AutoDELFIA System with Version 3.0 Software: Potential plate loading failures

Status: Terminated

Product Quantity: 1 unit (US) 2 units (OUS)

Code Information:

Batch Code: 649552 OUS: 649552, 649552

Distribution Pattern:

Worldwide Distribution - US Nationwide in the state of MN and countries of China, India, Philippines, France, South Korea, Vietnam, Taiwan, Morocco, Kazachstan, UK, Spain, and Israel,

Voluntary or Mandated:

Voluntary: Firm initiated