MobileDiagnost wDR, Model numbers 712001, 712002, 712004, 712006, and 712007
Reported: February 21, 2024 Initiated: October 14, 2021 #Z-1083-2024
Product Description
MobileDiagnost wDR, Model numbers 712001, 712002, 712004, 712006, and 712007
Reason for Recall
While cleaning or disinfecting the system, if the process is not followed as described in the manual and excessive liquid is used or sprayed directly on the system, it could cause a short circuit of the fine positioning control button. This would result in the system moving on its own in a very slow speed forward circular motion.
Details
- Recalling Firm
- SEDECAL SA
- Units Affected
- 851 devices
- Distribution
- US Nationwide distribution. There was government distribution but no military distribution.
- Location
- Algete, N/A
Frequently Asked Questions
What product was recalled? ▼
MobileDiagnost wDR, Model numbers 712001, 712002, 712004, 712006, and 712007. Recalled by SEDECAL SA. Units affected: 851 devices.
Why was this product recalled? ▼
While cleaning or disinfecting the system, if the process is not followed as described in the manual and excessive liquid is used or sprayed directly on the system, it could cause a short circuit of the fine positioning control button. This would result in the system moving on its own in a very slow speed forward circular motion.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 21, 2024. Severity: Moderate. Recall number: Z-1083-2024.
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