Reported Apr 30, 2025 · Ongoing
Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007…
Remote Diagnostic Technologies Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Remote Diagnostic Technologies Ltd. · Farnborough Aerospace Centre · Farnborough, N/A · N/A
Is this the product you have?
- Tempus Pro Patient Monitor
- REFs00-1004-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)]
- Lot codes and dates
- All Lots/ UDI-DI(s)
00-1004-R - 05060472440020 & 0506047244290100-1007-R - 05060472440013 & 0506047244291800-1024-R - 05060472441027 & 0506047244292500-1026-R - 05060472441058 & 0506047244293200-1004 - 0506047244062400-1007 - 05060472440655
- All Lots/ UDI-DI(s)
- Amount recalled
- 6,961 units
Where it was sold
Why it was recalled
software issue that causes an error screen on a portable vital signs monitor when attaching video Laryngoscope.
This product could cause temporary or reversible health problems — stop using it.
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