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

Recall Z-1249-2026 — Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.25GA Convenience Kit - XES VS0644.25-XES

U.S. FDA — Device Enforcement · United States · 2025-12-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1249-2026
Date of alert
2025-12-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Vortex Surgical Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
810123482917
Reported risk: There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.
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.