Ziehm Imaging solo FD Mobile Fluoroscopic C-arm
This recall has been terminated (originally issued February 23, 2017).
- Company
- Ziehm Imaging Inc
- Recall Initiated
- February 23, 2017
- Terminated
- December 11, 2019
- Recall Number
- Z-1893-2017
- Quantity
- US - 2 systems
- Firm Location
- Orlando, FL
- Official Source
- View on FDA website ↗
Reason for Recall
During Ziehm Imaging GmbH FDA inspection, the label for the Collimator and X-ray Control panel was missing the manufacturer date as part of the identification for certified component
Distribution
US Distribution to the states of : FL and CA. No devices listed in this recall where distributed any foreign /military/government consignees from the U.S.A.
Lot / Code Info
S/N 52199, 52108
Root Cause
Labeling design
Action Taken
Ziehm Imaging will bring defect into compliance: Customer Precautions: Therefore, as there is no identifiable risk to patients, users or third parties, the manufacturer Ziehm Imaging GmbH advises customers they may continue to operate the affected device until the labeling materials can be remediated. Please alert all staff members working with the device to this notification. Remedy: 1. You will contact customers and initiate the actions to correct the failure to comply issues. 2. You will affix the identification labels to the collimator and x-ray control panel. 3. You will replace the existing user manual with one that reflects the reference images of the labels with manufacturer date. If there are any questions or concerns regarding this product safety issue, please do not hesitate to contact our National Service Team for further information at Ziehm Imaging, Inc. Toll-Free: (866) 949-4346, Fax: (866) 839-7893 or E- Mail: customerservice@ziehm.com