Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1704-2019 — AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero Applicator 29cm PG Catalog Number:700106003 UPN: H7877001060030 (2)Solero Applicator 29cm PG US Catalog Number:700106003US UPN:H787700106003US0 Product Usage: The Solero Microwave Tissue Ablation (MTA) System and ac

U.S. FDA — Device Enforcement · United States · 2019-04-17 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1704-2019
Date of alert: 2019-04-17
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Angiodynamics Inc. (Navilyst Medical Inc.)
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 16480626

Reported risk: 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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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