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

Recall Z-2933-2020 — StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-RCV-AO US and 2. FR4A-RCV-A0 EU - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical current to create

U.S. FDA — Device Enforcement · United States · 2020-07-15 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2933-2020
Date of alert: 2020-07-15
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Stimwave Technologies Inc
Product category: device
Product type: Devices

Reported risk: The product contains a non-functional component not referenced in product labeling.

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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