Angiodynamics, Inc. recalls Solero Generator Refurbished PG, Item No. H78712740000D0, Catalog No. 12740000D

Recalled September 15, 2021 · FDA recall Z-2438-2021 · 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

8 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 PG, Item No. H78712740000D0, Catalog No. 12740000D

Manufacturer(s)

Angiodynamics, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →