Medical DeviceAug 28, 2019
Arcos Brand Name Burn Navigator Model Numbers: Catalog 1120, Burn Navigator H2 Catalog 1125 recall — FDA Z-2295-2019
Battery packs may heat up abnormally and ignite in rare instance.
Class IIFDA: TerminatedArcos, Inc.
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Arcos, Inc. 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.