Recall Register

Remote Diagnostic Technologies Ltd.: FDA recalls

FDA enforcement events from 2020 to 2025; export dated . The recall start date and FDA report date are separate fields. Read the recall classes.

FDA enforcement reports name Remote Diagnostic Technologies Ltd. as the recalling firm in 12 events. The events have 12 product records. The recalls started from 2020 to 2025. All the events are device recalls. By FDA enforcement events, Remote Diagnostic Technologies Ltd. is number 291 of 1,628 firms that have a page. Events that Remote Diagnostic Technologies Ltd. started: 2 in 2024 and 4 in 2025. For all FDA enforcement events, the count rose by 3.6%, from 1,773 in 2024 to 1,836 in 2025. Class II is 91.7% of its events and 73.7% of all FDA events.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

12 events, newest first.

FDA enforcement events of Remote Diagnostic Technologies Ltd.
InitiatedProduct (first record)TypeClassRecordsStatus
26 Nov 2025Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel IBP Module, REF: 01-2017. Used with User/Operator ManualDeviceClass II1Ongoing
30 May 2025Inseego 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-RDeviceClass II1Ongoing
16 Apr 2025Tempus 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)]DeviceClass II1Ongoing
15 Apr 2025Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007DeviceClass II1Ongoing
28 Oct 2024Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker modeDeviceClass III1Ongoing
9 May 2024Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator ManualDeviceClass II1Ongoing
24 Aug 2023Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used With Tempus Pro Video Laryngoscope, REF 01-2044DeviceClass II1Ongoing
8 May 2023Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020DeviceClass II1Ongoing
23 Feb 2023Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified personnel, for the attended or unattended monitoring of single or multiple vital signs in clinical and pre hospital care applications. The affected power supplies are related to the following Tempus…DeviceClass II1Ongoing
28 Jan 2022Tempus LS, Type DGE1, CAT 00-3010, REF 3.940590, Software version 1.3.5, UDI: (01)07613365001693DeviceClass II1Terminated
25 May 2021Tempus Pro - Patient physiological monitor, arrhythmia detector and alarm. Part No. - 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. Product Usage: intended to be used as a stand-alone monitor or as a telemedicine system (transmitting patient data to other medical professionals located elsewhere).DeviceClass II1Ongoing
17 Nov 2020Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.3.4 - Product Usage: The device is intended to be used in the following environmental: - Primarily in pre-hospital care and transport applications (including ambulances, fixed and rotary wing aircraft).DeviceClass II1Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

Remote Diagnostic Technologies Ltd.: events for each product type
TypeEvents
Device12
Remote Diagnostic Technologies Ltd.: events in each class
ClassEvents
Class II11
Class III1
Share of the events of the firm in Class I
0%
Share of all events on the register in Class I
18%
Events with the status Ongoing
10

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Remote Diagnostic Technologies Ltd., by the year that the recall started. The largest year is 2025, with 4 events.

Official channels

Cite this page

Recall Register. Remote Diagnostic Technologies Ltd.: FDA recalls. https://recallregister.com/firm/remote-diagnostic-technologies-ltd/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
3 Nov 2026
State of the firm address
N/A

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not rate one firm against another. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Remote Diagnostic Technologies Ltd. have?
Class II: 11 events. Class III: 1 event. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Remote Diagnostic Technologies Ltd.?
FDA event 97889, which the firm started on 26 Nov 2025. The first product in the record is: Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel IBP Module, REF: 01-2017. Used with User/Operator Manual
How many FDA recalls of Remote Diagnostic Technologies Ltd. have the status Ongoing?
10 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.