Remote Diagnostic Technologies recalls

Remote Diagnostic Technologies has 12 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 14 Jan 2026. 10 are still ongoing. 1 was reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls12since 2020

Last 12 months1reported

Class I00% of total

Ongoing10latest 14 Jan 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 1 0 0Feb 0 1 1May 0 0 1Aug 0 0 0Nov 0 1 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 11 92%Class III 1 8%

Why remote diagnostic technologies is recalled

Product types

By year

202618%
2025325%
2024217%
2023325%
202218%
202118%
202018%

Ongoing remote diagnostic technologies recalls

10 active

Reported	Class	Recall	Company	Reason	Where
14 Jan 2026Device	CLASS II	Philips Tempus Pro Patient Monitor recalled	Remote Diagnostic Technologies	Other	Nationwide
6 Aug 2025Device	CLASS II	Inseego USB8 Dongle Kit recalled by Remote Diagnostic Technologies	Remote Diagnostic Technologies	Device Malfunction	Nationwide
14 May 2025Device	CLASS II	Philips Tempus Pro Patient Monitor recalled	Remote Diagnostic Technologies	Labeling Errors	Nationwide
30 Apr 2025Device	CLASS II	Tempus Pro Patient Monitor, REFs recalled	Remote Diagnostic Technologies	Device Malfunction	Nationwide
4 Dec 2024Device	CLASS III	Tempus LS-Manual Defibrillator recalled	Remote Diagnostic Technologies	Labeling Errors	Nationwide
12 Jun 2024Device	CLASS II	Philips Tempus LS-Manual Defibrillator recalled	Remote Diagnostic Technologies	Other	Nationwide

All remote diagnostic technologies recalls, newest first

12 total

Reported	Class	Recall	Company	Reason	Where
14 Jan 2026Device	CLASS II	Philips Tempus Pro Patient Monitor recalled	Remote Diagnostic Technologies	Other	Nationwide
6 Aug 2025Device	CLASS II	Inseego USB8 Dongle Kit recalled by Remote Diagnostic Technologies	Remote Diagnostic Technologies	Device Malfunction	Nationwide
14 May 2025Device	CLASS II	Philips Tempus Pro Patient Monitor recalled	Remote Diagnostic Technologies	Labeling Errors	Nationwide
30 Apr 2025Device	CLASS II	Tempus Pro Patient Monitor, REFs recalled	Remote Diagnostic Technologies	Device Malfunction	Nationwide
4 Dec 2024Device	CLASS III	Tempus LS-Manual Defibrillator recalled	Remote Diagnostic Technologies	Labeling Errors	Nationwide
12 Jun 2024Device	CLASS II	Philips Tempus LS-Manual Defibrillator recalled	Remote Diagnostic Technologies	Other	Nationwide
27 Sep 2023Device	CLASS II	Philips Tempus Pro Patient Monitor recalled	Remote Diagnostic Technologies	Other	42 states
21 Jun 2023Device	CLASS II	Philips Tempus LS-Manual Defibrillator recalled	Remote Diagnostic Technologies	Device Malfunction	Nationwide
12 Apr 2023Device	CLASS II	Tempus Pro Patient Monitor is a portable vital signs recalled	Remote Diagnostic Technologies	Other	Nationwide
13 Apr 2022Device	CLASS II	Tempus LS, Type DGE1, CAT recalled by Remote Diagnostic Technologies	Remote Diagnostic Technologies	Hidden Drug Ingredients	Nationwide
7 Jul 2021Device	CLASS II	Tempus Pro - Patient physiological monitor recalled	Remote Diagnostic Technologies	Device Malfunction	Nationwide
23 Dec 2020Device	CLASS II	Tempus LS - Manual Defibrillator recalled	Remote Diagnostic Technologies	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.