Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Inseego USB8 4G Dongle Kit Recalled by Remote Diagnostic Technologies Ltd. Due to Kit USB flash drive contains outdated software, which...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Remote Diagnostic Technologies Ltd. directly.
Affected Products
Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an accessory to the Tempus Pro Monitor, REF: 00-1007-R, 00-1024-R, 00-1026-R
Quantity: 55
Why Was This Recalled?
Kit USB flash drive contains outdated software, which could result in reverting patient monitor to outdated software and reintroducing the video laryngoscope issue (related to an August 2023 recall), which could lead to delay in diagnosis, delayed treatment, hypoxia due to unexpected loss of video laryngoscopy and all other monitor measurements during system restart.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Remote Diagnostic Technologies Ltd.
Remote Diagnostic Technologies Ltd. has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report