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

Medtronic Disposable Pressure Display Sets: a) DLP¿ 114.3 cm (45 in), Model Number 61000; b) DLP¿ 114.3 cm (45 in), Model Number 62000 — recall Z-1802-2024

U.S. FDA — Device Enforcement · United States · 2024-03-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1802-2024
Date of alert
2024-03-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Perfusion Systems
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00643169880955
Reported risk: Potential for unsealed sterile packing.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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