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

Recall Z-0988-2022 — Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q

U.S. FDA — Device Enforcement · United States · 2022-03-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0988-2022
Date of alert
2022-03-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
St. Jude Medical, Cardiac Rhythm Management Division
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
111018237
Reported risk: Bluetooth malfunction impacting Gallant devices post-implant. The failure causes the device to enter an inductive-only telemetry mode with a loss of Bluetooth communication. The Bluetooth malfunction results in the inability to remotely monitor these devices and resulted in reduced battery longevity.
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.

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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.