Reported Sep 15, 2021 · Terminated

Solero Generator Refurbished US PG, Item No. H78712740000USD0, Catalog No. 12740000USD

Angiodynamics, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Angiodynamics, Inc. · 603 Queensbury Ave · Queensbury, NY · 12804-7619

Is this the product you have?

    • Solero Generator Refurbished US PG
    • Item No. H78712740000USD0
    • Catalog No. 12740000USD
Lot codes and dates
  • Serial Nos.
    • QBY0002546
    • QBY0002517
    • QBY0002525
    • QBY0002562
    • QBY0002669
    • QBY0002569
    • QBY0002382
    • QBY0002682
    • QBY0002561
    • QBY0002567
    • QBY0002580
    • QBY0002398
    • QBY0002379
    • QBY0002612
    • QBY0002708
    • QBY0002527
    • QBY0002758
    • QBY0002552
Amount recalled
16 US, 2 OUS

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 15, 2023 · Data as of Sep 19, 6:21 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.