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

Recall Z-2274-2023 — ACROBAT-i Vacuum Stabilizer System, Part Number C-OM-10000. Component of a chest stabilization system for cardiac and chest surgery.

U.S. FDA — Device Enforcement · United States · 2023-06-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2274-2023
Date of alert
2023-06-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Maquet Cardiovascular, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00607567700581
Reported risk: The Standard Blade may not securely latch onto the Activator Drive. This may result in the inability to stabilize and position or may result in the loss of stabilization and positioning of heart, release of device component into the patient, and/or a procedural delay and/or conversion.
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.