Intelli-C, Left side suspended Tabletop, REF: 03400010
FDA Recall Z-1669-2023 · Posted 2023-05-31
Advertisement
Recalling FirmNRT X-RAY A/S
Recall StatusOpen, Classified
Product CodeOWB
Date Initiated2023-04-27
Product Quantity13 units
Reason for Recall
There is a potential that the drive shaft in the detector up/down (IDE) movement of the X-Ray machine may break which causes the detector to move until it is stopped by the movement end-stop.
Firm Action
Between the dates of April 27, 2023 - May 1, 2023, NRT X-Ray A/S issued a "urgent: Medical Device Correction" via E-Mail to affected consignees. Per the customer communication, NRT ask consignees to take the following actions:
Step 1 Short term action
The first step of the recall is a corrective action which requires the existing fixation bracket components to be removed. Service Providers of the Intelli-C systems should follow the instructions in page 4 through 7 of the communication and report back to NRT using the Customer Response Card on page 8. The process is coordinated through US dealer Alpha Imaging in Willoughby, Ohio.
Step 2 Long term action
The second step is a preventive action to replace the IDE drive shaft and relating components. A separate set of instructions for this action will be provided in May together with the required parts for the replacement. These instructions will include a separate acknowledgement form for this action.
If you have questions regarding the contents of this letter, please contact your local Service provider or contact NRT X-RAY A/S directly using the following contact information:
Email: [email protected]
Phone: +45 2055 3309
Monday through Friday, (03:00)-11:00 Eastern Standard Time
(9:00 AM to 5:00 PM, Central European Time)
Root Cause
Device Design
Distribution Pattern
US Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, LA, NV, NY.
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.
Advertisement