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Terminated

DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray imaging system used in hospitals, clinics and medical practices by physicists, radiographers and radiologists to make, process and view static X-Ray radiographic images of the skeleton (including skull, spinal column and extremities), chest, abdomen and other body parts on adult, pediatric or neonatal patients.

FDA Recall Z-0692-2019 · Posted None

Recalling FirmAgfa-Gevaert, N.V.
Recall StatusTerminated
Product CodeKPR
Date Initiated2018-12-04
Date Terminated2020-04-24
Product Quantity10

Reason for Recall

After an upgrade of the software of the Overhead Tube Crane, there were isolated cases in which the Overhead Tube Crane movement does not stop when the movement button is released. Instead of stopping while the movement button is released, the Tube Head Crane moves to the intended position.

Firm Action

An Urgent Field Safety Notice dated 12/4/18 was sent to customers. Actions undertaken by Agfa: Soon Agfa or its representative will visit your site and install the latest revision of the hardware board, which will prevent a movement without user interaction. Recommended actions to be taken by you: If you notice an Overhead Tube Crane movement without user interaction, notify your Agfa Service contact at once. Please distribute this information within your facility to all those who need to be aware of it. It is important to take the actions detailed in this Urgent Field Safety Notification and to acknowledge receipt of this notification.

Root Cause

Software design

Distribution Pattern

US Nationwide Distribution in the states: IN, KS, MA, SC, and VA.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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