Recall StatusTerminated
Date Initiated2018-04-18
Date Terminated2021-05-13
Product Quantity43
Reason for Recall
It was found when an operator performs a radiography using the wireless flat panel detector (FPD), a message window was displayed on the monitor stating image transmission was not completed and there was no image. It also showed the OK button to reacquire image data form the FPD, and the Cancel button to cancel the reacquisition.
When the operator selects the OK button, the same message window appears. The operator then repeated the same operation several times and finally selected the Cancel button to quit the reacquisition mode.
Firm Action
On 04/18/2018, the firm mailed Urgent: Medical Device Correction letters via USPS return receipt mail. The letter contains a return reply form that is to be faxed. After one month contact will be made with each non-responding location and a copy of the letter will be faxed to that location and the fax receipt will serve as proof of notification.
Upon release of the modified software it will be assigned to a firm employee with instructions for implementation at each site. Each incident is assigned unique service incident (case) and the completion of the service incidents are tracked through completion. In the event that a customer refuses the installation the customer would be requested to sign a service case record stating that the corrected software was refused.
Root Cause
Software design
Distribution Pattern
Domestic: AR, FL, GA, PA, IL, LA, MI, NC, NJ, NY, OH, TN, TX, UT, VT, WI, and WV
Foreign: Australia, Canada, The Netherlands, South Korea, and Malaysia
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.