Recalls / —

—#203644

Product

DigitalDiagnost C90 Release 3.1, used to acquire, process, store, display and export digital radiographic images.

FDA product code

JAA — System, X-Ray, Fluoroscopic, Image-Intensified

Device class

Class 2

Medical specialty

Radiology

510(k) numbers

K210692

Affected lot / code info

Model No. 712026; Serial No. SN14000197 & SN14000260.

Why it was recalled

Potential for units suspended on the ceiling to fail and fall.

Root cause (FDA determination)

Under Investigation by firm

Action the firm took

The firm distributed recall notifications dated 8/31/2023 via FedEx to affected consignees. Consignees are instructed to immediately stop use of affected devices and contact their local Philips service representative if the Ceiling Suspension becomes unstable, if moving the Ceiling Suspended X-Ray Tube requires a high amount of force, or if moving the Ceiling Suspended X-Ray Tube is noticeably hampered. The recall notice is to be circulated among all device users, so they are aware of this issue and placed as an addendum in the IFU. Consignees are to complete the provided response form and return it to Philips no later than 30 days from notification receipt via email to pd.cnr@philips.com. Philips will contact consignees to schedule a time for a Field Service Engineer to visit customer sites to inspect affected systems and correct the issue. Consignees with any questions are to contact the Customer Care Solutions Center at 1-800-722-9377.

Recalling firm

Firm

Philips North America Llc

Address

222 Jacobs St, Cambridge, Massachusetts 02141-2289

Distribution

Distribution pattern

Nationwide distribution.

Timeline

Recall initiated

2023-09-21

Posted by FDA

2023-11-08

Status

—

Source: openFDA Device Recall endpoint. Recall record ID #203644. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.