RecallDepth

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

Company
Angiodynamics, Inc.
Recall Initiated
July 20, 2021
Terminated
March 15, 2023
Recall Number
Z-2438-2021
Quantity
8 OUS
Firm Location
Queensbury, NY

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.

Distribution

Domestic distribution Nationwide. Foreign distribution worldwide.

Lot / Code Info

Serial Nos. QBY0002816 QBY0002817 QBY0002348 QBY0002308 QBY0002311 QBY0002711 QBY0002741 QBY0002858

Root Cause

Software design

Action Taken

On July 20, 2021, the firm initiated the recall by issuing Urgent Voluntary Medical Device Recall letters to affected consignees. Customers were informed of the software upgrade. Customers were asked to return their generators to AngioDynamics for service. The firm's Hardware Service Department will contact you to schedule the upgrade, which may include the shipment of a replacement generator to your facility if needed to be used during the upgrade of your devices. In the interim, while this upgrade is being scheduled, you may continue to use the Solero generator and are instructed to adhere to the following Warning in the current product labeling (User Manual): WARNING: Do not initiate the procedure/anesthesia until the applicator has been connected, primed, and the generator status bar indicates "Ready".

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