RecallDepth

BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit format 453560824741 453560829261;

This recall is currently active, issued February 2, 2024. It was issued by Philips North America.

Company
Philips North America
Recall Initiated
December 15, 2023
Posted
February 2, 2024
Recall Number
Z-0930-2024
Quantity
56 US; 46 OUS
Firm Location
Cambridge, MA
Official Source
View on FDA website ↗

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.

Distribution

Domestic distribution nationwide. International distribution worldwide.

Lot / Code Info

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

Root Cause

Component design/selection

Action Taken

On December 15, 2023, the firm notified affected customers via URGENT Medical Device Correction letters. Customers were instructed to not position a patient's lower limbs directly under the detector below the Center of Gantry bore. Customers should circulate the notice to all users of the device for awareness and retain the letter with affected systems until the correction is complete. Philips will contact customers to schedule a time for a Philips Field Service Engineer (FSE) to visit the customer site and correct the system if necessary. If you need any further information or support concerning this issue, please contact the Customer Care Solutions Center (1-800-722-9377). As of 3/14/24, Philips will begin inspecting all affected devices in the field to ensure alignment of the radial leadscrew. Systems that are identified as having a misaligned leadscrew will undergo a report. Additionally, Philips will begin intsallation of a secondary catching mechanism (safety plate) starting in May 2024 in all devices. The firm will contact customers to coordinate these activities.

More recalls by Philips North America

View all recalls by this company →