FDA Device recall Z-2436-2021
Solero Generator Refurbished US PG, Item No. H78712740000USD0, Catalog No. 12740000USD
- FDA Device
- Class II
- terminated
- Published 2021-09-15
On 2021-09-15 the FDA classified a Class II recall of Solero Generator Refurbished US PG, Item No. H78712740000USD0, Catalog No. 12740000USD by Angiodynamics, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2436-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-07-20 |
| Published | 2021-09-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Angiodynamics |
| Distribution | US |
Product
Solero Generator Refurbished US PG, Item No. H78712740000USD0, Catalog No. 12740000USD
Reason
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.
Identifiers
| code_info | Serial Nos. QBY0002546 QBY0002517 QBY0002525 QBY0002562 QBY0002669 QBY0002569 QBY0002382 QBY0002682 QBY0002561 QBY00025…Serial Nos. QBY0002546 QBY0002517 QBY0002525 QBY0002562 QBY0002669 QBY0002569 QBY0002382 QBY0002682 QBY0002561 QBY0002567 QBY0002580 QBY0002398 QBY0002379 QBY0002612 QBY0002708 QBY0002527 QBY0002758 QBY0002552 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2436-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.