Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Optum Nimbus II Plus Recalled by OptumHealth Care Solutions LLC Due to Nimbus II Plus, Infusion Pump Systems, manufactured by...

Date: April 18, 2024
Company: OptumHealth Care Solutions LLC
Status: Ongoing
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 OptumHealth Care Solutions LLC directly.

Affected Products

Optum Nimbus II Plus, Model number AAA-00170; Ambulatory Infusion Pump

Quantity: 208 units

Why Was This Recalled?

Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being removed the from the market due to multiple potential failure modes, including battery failure, upstream occlusion, system errors, drug product leakage, high or low flow rate, or damaged pump housing.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About OptumHealth Care Solutions LLC

OptumHealth Care Solutions LLC has 1 total recall tracked by RecallDetector.

Related Recalls

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