Philips Electronics North America Corporation: Medical Device Recall in 2017 - (Recall #: Z-1820-2017)

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:

Allura Xper Release 8.2 (Laird chiller is always installed); Allura Xper FD10 722026; Allura Xper FD10/10 722027; Allura Xper FD20/10 biplane 722029; Allura Xper FD10 OR Table 722033; Allura Xper FD10/10 OR Table 722034; Allura Xper FD20/10 OR Table 722036; Allure Xper FD20/20 722038; Allura Xper FD20/20 biplane OR Table 722039

Product Classification:

Class II

Date Initiated: March 22, 2017

Date Posted: April 26, 2017

Recall Number: Z-1820-2017

Event ID: 76810

Reason for Recall:

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.

Status: Terminated

Product Quantity: 6992 (total for all devices)

Code Information:

Devices with Laird Chiller.

Distribution Pattern:

Nationwide, worldwide including Canada

Voluntary or Mandated:

Voluntary: Firm initiated