FDA Device recall Z-1701-2019
AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero Generator Refurbished PG Catalog Number: 12740000D UPN: H7871274000…
- FDA Device
- Class II
- terminated
- Published 2019-06-12
On 2019-06-12 the FDA classified a Class II recall of AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero Generator Refurbished PG Catalog Number: 12740000D UPN: H7871274000… by Angiodynamics Navilyst Medical, citing updated Warning Statements in the Operator's Manual/Directions for Use and Software Updates to reduce the risk of potential patient harm due to a delay in performing a procedure.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1701-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-04-17 |
| Published | 2019-06-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Angiodynamics Navilyst Medical |
| Distribution | US |
Product
AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero Generator Refurbished PG Catalog Number: 12740000D UPN: H78712740000D0 (2) Solero Generator Refurbished US PG Catalog Number: 12740000USD ;UPN: H78712740000USD0
Reason
Updated Warning Statements in the Operator's Manual/Directions for Use and Software Updates to reduce the risk of potential patient harm due to a delay in performing a procedure
Identifiers
| code_info | Serial Numbers: (1) QBY0002025 QBY0002027 QBY0001994 QBY0001993 QBY0002001 QBY0002006 QBY0002008 QBY0002002…Serial Numbers: (1) QBY0002025 QBY0002027 QBY0001994 QBY0001993 QBY0002001 QBY0002006 QBY0002008 QBY0002002 QBY0002003 QBY0002007 QBY0002010 QBY0002004 QBY0002036 QBY0002040 QBY0002042 QBY0002044 QBY0002039 QBY0002035 QBY0002034 QBY0002033 QBY0002026 QBY0002041 QBY0002037 QBY0002051 QBY0002052 QBY0002055 QBY0002054 QBY0002058 QBY0002056 QBY0002301 QBY0002059 QBY0002311 QBY0002352 QBY0002429 QBY0002478 QBY0002529 QBY0002628 QBY0002695 QBY0002696 QBY0002698 QBY0002710 QBY0002711 QBY0002740 QBY0002742 QBY0002741 QBY0002778 QBY0002795 QBY0002820 QBY0002818 QBY0002811 QBY0002834 QBY0002827 QBY0002828 QBY0002829 QBY0002830 QBY0002831 QBY0002836 QBY0002838 QBY0002843 QBY0002844 QBY0002859 QBY0002860 QBY0002926 QBY0002927 QBY0002936 QBY0002909 QBY0002935 QBY0002937 QBY0002938 QBY0003040 QBY0003162 QBY0003185 QBY0003215 QBY0003216 QBY0003135 QBY0003137 QBY0003141 (2) Lot/Serial Number QBY0002279 QBY0002294 QBY00 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1701-2019%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.