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

Recall Z-2693-2020 — Accurian RF Ablation, Cannula pk, Accurian, 150mm, 20G, 10mm, CS Product Number: AC0012 GTIN / UPN: 20763000153629 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting, and a stylet with a

U.S. FDA — Device Enforcement · United States · 2020-06-08 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2693-2020
Date of alert: 2020-06-08
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Medtronic Sofamor Danek USA Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 20763000153629

Reported risk: Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.

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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