Reported Apr 26, 2017 · Terminated

The following systems are only affected if a Laird chiller is installed (11NC

Philips Electronics North America Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips Electronics North America Corporation · 3000 Minuteman Rd · Andover, MA · 01810-1032

Is this the product you have?

The following systems are only affected if a Laird chiller is installed (11NC

17 of 17 products

Products covered by this recall
#Product as published
198960021599): Allura Xper Releases 3 to 8.1: Allura Xper FD10 (C+F). 722003
2Allura Xper FD10/10 722005
3Allura Xper FD20 722006
4Allura Xper FD20/10 and FD20/20 722008
5Allura Xper FD10 722010
6Allura Xper FD10/10 722011
7Allura Xper FD20 722012
8Allura Xper FD20 biplane 722013
9Allura Xper FD10 OR Table 722014
10Allura Xper FD20 OR Table 722015
11Allura Xper FD10/10 OR Table 722019
12Allura Xper FD20 Biplane OR Table 722020
13Allura Xper FD10 OR Table 722022
14Allura Xper FD20 OR Table 722023
15Allura Xper FD10/10 OR Table 722024
16Allura Xper FD20 Biplane OR Table 722025
17Allura CV20 722031
Lot codes and dates
  • Devices with a Laird Chiller.
Amount recalled
6992 (total distributed for all products)

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

Due to a leak in the detector cooling system, cooling liquid may leak outside the drip tray of the chiller. If this occurs the liquid may drip onto electrical components in the R cabinet located in the technical room, which could lead to damage to the system and potentially cause thermal events such as a burning odor, smoke or fire.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 17, 2021 · Data as of Sep 19, 6:04 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.