Angiodynamics, Inc.: Medical Device Recall in 2021 - (Recall #: Z-2438-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 20, 2021

Date Posted: September 15, 2021

Recall Number: Z-2438-2021

Event ID: 88444

Reason for Recall:

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.

Status: Terminated

Product Quantity: 8 OUS

Code Information:

Serial Nos. QBY0002816 QBY0002817 QBY0002348 QBY0002308 QBY0002311 QBY0002711 QBY0002741 QBY0002858

Distribution Pattern:

Domestic distribution Nationwide. Foreign distribution worldwide.

Voluntary or Mandated:

Voluntary: Firm initiated