Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Tempus Pro Patient Monitor Recalled by Remote Diagnostic Technologies Ltd. Due to software issue that causes an error screen on...
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
Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007 (Tempus Pro non-printer, IBP, with headset dock), 00-1024-R (Tempus Pro printer), 00-1026-R (Tempus Pro printer, IBP), 00-1007 [(Tempus Pro, BT Dock (IB Only)], 00-1004 00-1004 [Tempus Pro (IB Only)]
Quantity: 6,961 units
Why Was This Recalled?
software issue that causes an error screen on a portable vital signs monitor when attaching video Laryngoscope.
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