Class II — Potential Health Hazard

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

OrganOx metra -Intended as a Normothermic Machine Perfusion system of Recalled by OrganOx Ltd Due to Battery movement led to damage of one of...

Date: October 15, 2024
Company: OrganOx Ltd
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 OrganOx Ltd directly.

Affected Products

OrganOx metra -Intended as a Normothermic Machine Perfusion system of donor transport livers. Model/Catalog Number: D0003 The OrganOx metra is a transportable device intended to be used to sustain donor livers destined for transplantation in a functioning state for a total preservation time of up to 12 hours.

Quantity: 20 units

Why Was This Recalled?

Battery movement led to damage of one of the battery cells causing it to short to the battery retention bracket

Where Was This Sold?

This product was distributed to 1 state: DC

Affected (1 state)Not affected

About OrganOx Ltd

OrganOx Ltd has 1 total recall tracked by RecallDetector.

Related Recalls

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