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

Recall Z-1007-2024 — ExcelsiusGPS Cannula A, 9mm x 250mm, Cannula used with ball tip probes, Model No. 6143.2844

U.S. FDA — Device Enforcement · United States · 2023-12-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1007-2024
Date of alert
2023-12-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Globus Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00889095998498
Reported risk: Devices may not be rendered sterile due to an internal gap that may be present on some devices causing increased difficulty cleaning prior to steam sterilization. There is an increased risk for infection, inflammation, local toxicity, systemic toxicity, sensitivity, and cross-contamination.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.