Philips North America Llc: Medical Device Recall in 2022 - (Recall #: Z-0725-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a Laird chiller without an extended drip tray: Model Number: 722031

Product Classification:

Class II

Date Initiated: November 24, 2021

Date Posted: March 16, 2022

Recall Number: Z-0725-2022

Event ID: 89375

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: Ongoing

Product Quantity: 1 unit

Code Information:

S/N: OUS 109

Distribution Pattern:

US Nationwide Foreign: Argentina Austria Bangladesh Brazil Chile China Denmark Dominican Republic France Germany Greece India Indonesia Iran Israel Italy Japan Korea, Republic of Malaysia Mexico Netherlands Philippines Russian Federation Saudi Arabia South Africa Spain Sri Lanka Switzerland Taiwan Thailand Turkey United Kingdom Virgin Islands (U.S.)

Voluntary or Mandated:

Voluntary: Firm initiated