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

Recall Z-2482-2025 — DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12115 LV VENT 15FR, Model Number 12115

U.S. FDA — Device Enforcement · United States · 2025-08-06 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2482-2025
Date of alert
2025-08-06
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Medtronic Perfusion Systems
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
20643169880935
Reported risk: The catheters may not retain their shape.
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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