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Angiodynamics, Inc. recalls Solero Generator Refurbished US PG, Item No. H78712740000USD0, Catalog No. 12740000USD
Recalled September 15, 2021 · FDA recall Z-2436-2021 · Angiodynamics
Hazard
Specific serial numbers of the Solero MTA Generator require servicing to upgrade the software to help reduce the incidence of Error 0001, which can occur during system start-up. · FDA Class II
Units
16 US, 2 OUS
Sold at
Domestic distribution Nationwide. Foreign distribution worldwide.
Description
Specific serial numbers of the Solero MTA Generator require servicing to upgrade the software to help reduce the incidence of Error 0001, which can occur during system start-up.
Product
Solero Generator Refurbished US PG, Item No. H78712740000USD0, Catalog No. 12740000USD
Manufacturer(s)
Angiodynamics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →