Philips North America: Medical Device Recall in 2024 - (Recall #: Z-0929-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791 453560279811 453560279801; 4x4 digit format 2170-3000A 2170-3001A 2170-3002A 2170-3003A

Product Classification:

Class I

Date Initiated: December 15, 2023

Date Posted: February 14, 2024

Recall Number: Z-0929-2024

Event ID: 93767

Reason for Recall:

Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation. If detector is positioned above center of gantry, there may be an interruption to normal system operation.

Status: Ongoing

Product Quantity: 302 US; 264 OUS

Code Information:

All serial numbers are affected. No UDI-DI available for this product.

Distribution Pattern:

Domestic distribution nationwide. International distribution worldwide.

Voluntary or Mandated:

Voluntary: Firm initiated