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MEDLINE INDUSTRIES, INC. · Model HNX19100 · UDI-DI 10197344039746

PTI Prescription
10
510(k) clearances
154
Adverse events
12
Recalls
33
Facilities

Description

HUBER INFUSION SET,NO Y-SITE,19G X 1

Recalls

DateFirmReason
2020-06-19Becton Dickinson & CompanyPotential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure
2020-06-19Becton Dickinson & CompanyPotential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure
2020-06-19Becton Dickinson & CompanyPotential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure
2020-06-19Becton Dickinson & CompanyPotential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure
2020-06-19Becton Dickinson & CompanyPotential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure
2020-06-19Becton Dickinson & CompanyPotential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure
2020-06-19Becton Dickinson & CompanyPotential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure
2020-06-19Becton Dickinson & CompanyPotential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure
2020-06-19Becton Dickinson & CompanyPotential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure
2020-06-19Becton Dickinson & CompanyPotential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.