OrganOx metra -Intended as a Normothermic Machine Perfusion system of donor transport livers recall — FDA Z-0501-2025
Battery movement led to damage of one of the battery cells causing it to short to the battery retention bracket
Overview of recall records associated with OrganOx Ltd, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Battery movement led to damage of one of the battery cells causing it to short to the battery retention bracket
This page summarizes recall records in which the official source identifies OrganOx Ltd as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.