Recall Register

Food, drugs, devices › Firms

Spacelabs Healthcare, Ltd.

FDA recalling firm · 5 enforcement events · 6 product records · 2017–2025 · N/A

Spacelabs Healthcare, Ltd. has 5 FDA enforcement events on this register (6 product records) between 2017 and 2025: 5 device; the busiest year was 2017 with 1.

40% of its events are Class I; the most common class is Class II (3). 2 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
16 Sep 2025Brand Name: Sentinel V11 Product Name: Sentinel V11 Model/Catalog Number: 92810 Software Version: 11.6.0 Product Description: Cardiology Information Management System Component: No The Sentinel Cardiology Information Management System is intended to connect to supported medical devices and analyzers in order to…DeviceClass II1Ongoing
25 Nov 2024Eclipse PRO REF 98700 The Spacelabs model 98700 is a portable non-invasive Holter recorder intended to record the patient s ambulatory electrocardiogram.DeviceClass II2Ongoing
6 Nov 2020Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is easy to install and to use.DeviceClass II1Terminated
11 Jul 2018Arkon Anesthesia Delivery System with Arkon Software Version 2.70, Display Unit Assembly 650-1769-00 installed, and Model #: 99999. This system includes a ventilator. The Spacelabs Arkon Anesthesia Workstation is intended for use in the hospital environment and operating room. It may be used for the delivery of…DeviceClass I1Terminated
11 Oct 2017Arkon Anesthesia Delivery System, Model 99999, and software version 2.61 and upgrade kit 050-9043-00 Rev G. The Spacelabs Arkon Anesthesia Workstation is intended for use in the hospital environment and operating room. It may be used for the delivery of oxygen, air and nitrous oxide in a controlled manner to various…DeviceClass I1Terminated

By type and class

Device5
Class II3
Class I2

Class I: 40% of this firm's events; 18% of all events on the register.

Events by year

17
18
19
20
21
22
23
24
25
26
Enforcement events for Spacelabs Healthcare, Ltd. by year initiated.

Questions and answers

How many FDA recalls has Spacelabs Healthcare, Ltd. had?

5 enforcement events (6 product records) on this register, 2017–2025: 5 device.

Are any Spacelabs Healthcare, Ltd. recalls ongoing?

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

What class are Spacelabs Healthcare, Ltd. recalls?

3 Class II, 2 Class I. 40% 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.