Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Spacelabs Healthcare elance Vital Signs Monitor Recalled by Spacelabs Healthcare, Llc Due to Spacelabs Healthcare elance Vital Signs Monitor with Option...

Date: October 17, 2013
Company: Spacelabs Healthcare, Llc
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Spacelabs Healthcare, Llc directly.

Affected Products

Spacelabs Healthcare elance Vital Signs Monitor, Model 93300, with Option S. It is a patient monitor with arrhythmia detection or alarms.

Quantity: 89 units total (1 in US and 88 International)

Why Was This Recalled?

Spacelabs Healthcare elance Vital Signs Monitor with Option S, model 93330, is recalled because the monitor will not permit connection of any of the Spacelabs TruLink line of SpO2 sensors.

Where Was This Sold?

Worldwide Distribution-Distributed in Puerto Rico and the countries of France, Indonesia, Korea, Nicaragua, Philippines, and Taiwan.

About Spacelabs Healthcare, Llc

Spacelabs Healthcare, Llc has 10 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report