Becton Dickinson Infusion Therapy Systems recalls

Becton Dickinson Infusion Therapy Systems has 15 recalls on record with the FDA and USDA, the earliest in 2021 and the latest reported on 2 Jul 2025. 15 are still ongoing. The most frequent reason is device malfunction.

Total recalls15since 2021
Last 12 months0reported
Class I00% of total
Ongoing15latest 2 Jul 2025

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 15 100%Class III 0 0%

Why becton dickinson infusion therapy systems is recalled

Product types

By year

Ongoing becton dickinson infusion therapy systems recalls

15 active

All becton dickinson infusion therapy systems recalls, newest first

15 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIREF: 382633, BD Insyte Autoguard BC Winged recalledBecton Dickinson Infusion Therapy SystemsDevice MalfunctionNationwide
DeviceCLASS IIREF: 381811, BD Insyte Autoguard BC Pro Winged Shielded IV Catheter recalledBecton Dickinson Infusion Therapy SystemsDevice MalfunctionNationwide
DeviceCLASS IIREF: 381533, BD Insyte Autoguard Winged, Shielded IV Catheter, 20 GA recalledBecton Dickinson Infusion Therapy SystemsDevice MalfunctionNationwide
DeviceCLASS IIREF: 382944, BD Insyte Autoguard BC Pro Winged Shielded IV Catheter recalledBecton Dickinson Infusion Therapy SystemsDevice MalfunctionNationwide
DeviceCLASS IIREF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA recalledBecton Dickinson Infusion Therapy SystemsDevice MalfunctionNationwide
DeviceCLASS IIREF: 381433, BD Insyte Autoguard Shielded IV Catheter recalledBecton Dickinson Infusion Therapy SystemsDevice MalfunctionNationwide
DeviceCLASS IIREF: 382544 BD Insyte Autoguard Shielded IV Catheter recalledBecton Dickinson Infusion Therapy SystemsDevice MalfunctionNationwide
DeviceCLASS IIREF: 381923 BD Insyte Autoguard Winged Shielded IV Catheter, 22 GA recalledBecton Dickinson Infusion Therapy SystemsDevice MalfunctionNationwide
DeviceCLASS IIREF: 381434 BD Insyte Autoguard Shielded IV Catheter recalledBecton Dickinson Infusion Therapy SystemsDevice MalfunctionNationwide
DeviceCLASS IIBD Cathena Safety IV Catheter BD Multiguard Technology recalledBecton Dickinson Infusion Therapy SystemsPackaging DefectsNationwide
DeviceCLASS IIBD Insyte Autoguard BC, Shielded IV Catheter recalledBecton Dickinson Infusion Therapy SystemsPackaging DefectsIL
DeviceCLASS IIBD Insyte Autoguard BC Shielded IV Catheter recalledBecton Dickinson Infusion Therapy SystemsPackaging DefectsNationwide
DeviceCLASS IIREF: 386862, BD Cathena Safety IV catheter with BD Multiguard recalledBecton Dickinson Infusion Therapy SystemsDevice MalfunctionNationwide
DeviceCLASS IIBD Nexiva Closed IV Catheter System - Single Port recalledBecton Dickinson Infusion Therapy SystemsOther13 states
DeviceCLASS IIBD Nexiva/hr./min recalled by Becton Dickinson InfusionBecton Dickinson Infusion Therapy SystemsSterilityNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.