Recall Register

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Remote Diagnostic Technologies Ltd.

FDA recalling firm · 12 enforcement events · 12 product records · 2020–2025 · N/A

Remote Diagnostic Technologies Ltd. has 12 FDA enforcement events on this register (12 product records) between 2020 and 2025: 12 device; the busiest year was 2025 with 4.

0% of its events are Class I; the most common class is Class II (11). 10 events are listed as ongoing; the recalling firm's address is in N/A.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

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

By type and class

Device12
Class II11
Class III1

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

20
21
22
23
24
25
26
Enforcement events for Remote Diagnostic Technologies Ltd. by year initiated.

Questions and answers

How many FDA recalls has Remote Diagnostic Technologies Ltd. had?

12 enforcement events (12 product records) on this register, 2020–2025: 12 device.

Are any Remote Diagnostic Technologies Ltd. recalls ongoing?

10 events are listed as ongoing in the current openFDA export.

What class are Remote Diagnostic Technologies Ltd. recalls?

11 Class II, 1 Class III. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.