Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0692-2019 — 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 ske

U.S. FDA — Device Enforcement · Belgium · 2018-12-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0692-2019
Date of alert: 2018-12-04
Country / jurisdiction: Belgium
Risk level: Class II
Risk type: recall
Brand: Agfa-Gevaert, N.V.
Product category: device
Product type: Devices

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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