DigitalDiagnost C90, Model No. 712034 and 712035
Reported: July 5, 2023 Initiated: May 19, 2023 #Z-2042-2023
Product Description
DigitalDiagnost C90, Model No. 712034 and 712035
Reason for Recall
There is a software login in issue that may prevent the user from logging in.
Details
- Recalling Firm
- Philips North America Llc
- Units Affected
- 58
- Distribution
- Distribution in US: AZ, GA, IN, IA, MN, NE, NH, OH, TX OUS distribution to Australia, Chile, China, Malta, Namibia, New Zealand, Oman, Panama, Qatar, Suriname, United Kingdom
- Location
- Cambridge, MA
Frequently Asked Questions
What product was recalled? ▼
DigitalDiagnost C90, Model No. 712034 and 712035. Recalled by Philips North America Llc. Units affected: 58.
Why was this product recalled? ▼
There is a software login in issue that may prevent the user from logging in.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 5, 2023. Severity: Moderate. Recall number: Z-2042-2023.
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