FDA Device Intelligence
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Non-Coring (Huber) Needle

FDA product code PTI · Class 2 · General Hospital

126
Registered devices
154
Adverse events
12
Recalls
13
510(k) clearances

Devices with this code

Recent 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 re
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 re
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 re
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 re
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 re
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 re
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 re
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 re
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 re
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 re

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.