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SURECAN SAFETY II

B. BRAUN MEDICAL INC. · Model 4447007-02 · UDI-DI 04046964999840

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

Description

Surecan™ Safety II Port Access Needle Set 20G x 1 in. (25mm)

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.