PlainRecalls

Remote Diagnostic Technologies Ltd.

Compiled from official public sources by the publisher.

12 recalls on record · Latest: Jan 14, 2026

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Agency notice ledger

Federal filing book Remote Diagnostic Technolog… LIGHT-BOOK · SINGLE-AGENCY

#1,285 of 14,151 · 12 notices · 0.011% archive

  • BOOK 12 notices
  • RANK #1,285 of 14,151
  • SHARE 0.011% archive
  • AGENCY FDA Devices (12)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jan 14, 2026
  • PHOTO 2k Innovations Inc.

Nearest notice-volume peer: 2k Innovations Inc. (0 notice gap)

Remote Diagnostic Technologies Ltd. accounts for about 0.011% of the 104,423-notice archive on 12 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Remote Diagnostic Technolog… sits among 14,151 recalling firms

Remote Diagnostic Technologies Ltd. ranks 1,285th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Remote Diagnostic Technolog… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

12 1285th of 14151 higher than 12,841 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Remote Diagnostic Technolog… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Remote Diagnostic Technologies Ltd. holds about 0.011% of archive notices alongside 12 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jan 14, 2026

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
FDA Devices Moderate Aug 6, 2025

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
FDA Devices Moderate May 14, 2025

Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007
FDA Devices Moderate Apr 30, 2025

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)]
FDA Devices Low Dec 4, 2024

Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode
FDA Devices Moderate Jun 12, 2024

Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual
FDA Devices Moderate Sep 27, 2023

Philips 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 01-2044
FDA Devices Moderate Jun 21, 2023

Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
FDA Devices Moderate Apr 12, 2023

Tempus 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 Pro Patient Monitoring units: Model Numbers: 00-1004 00-1004-R 00-1007 00-1007-R 00-1024-R 00-1026-R Model Numbers: 00-1004 00-1004-R 00-1007 00-1007-R 00-1024-R 0
FDA Devices Moderate Apr 13, 2022

Tempus LS, Type DGE1, CAT 00-3010, REF 3.940590, Software version 1.3.5, UDI: (01)07613365001693
FDA Devices Moderate Jul 7, 2021

Tempus 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).
FDA Devices Moderate Dec 23, 2020

Tempus 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).

Remote Diagnostic Technolog… holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (12 here — thin-book).

2k Innovations Inc. 12 3fish Inc. 12 Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. 12 Agfa Healthcare Corp. 12 Amgen, Inc. 12

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

2k Innovations Inc. 12 Agfa Healthcare Corp. 12 Boston Scientific 12 Cepheid 12

Frequently Asked Questions

How many federal recall notices name Remote Diagnostic Technolog…? ▼
PlainRecalls indexes 12 distinct federal recall events naming Remote Diagnostic Technologies Ltd., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Remote Diagnostic Technolog… sit among other recalling firms? ▼
Remote Diagnostic Technologies Ltd. ranks #1,285 of 14,151 by distinct recall-event count among 14,151 firms in this archive (91st percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Remote Diagnostic Technolog…'s notices? ▼
FDA Devices accounts for 12 of this firm's 12 indexed notices.
What product category dominates Remote Diagnostic Technolog…'s filing book? ▼
Filings for Remote Diagnostic Technologies Ltd. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Remote Diagnostic Technologies Ltd.: 12 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Remote Diagnostic Technologies Ltd.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026