Becton Dickinson recalls

Becton Dickinson has 364 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 10 Jun 2026. 111 are still ongoing. 24 were reported in the last 12 months.

Total recalls364since 2012
Last 12 months24reported
Class I164% of total
Ongoing111latest 10 Jun 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 16 4%Class II 335 92%Class III 13 4%

Why becton dickinson is recalled

By year

Ongoing becton dickinson recalls

111 active

All becton dickinson recalls, newest first

364 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IBD¿Spinal Tray with BD¿Whitacre Needle recalled by Becton Dickinson &Becton DickinsonProcessing DeviationNationwide
DeviceCLASS IBD¿Spinal Tray with BD¿Whitacre Needle recalled by Becton Dickinson &Becton DickinsonProcessing DeviationNationwide
DeviceCLASS IBD¿Spinal Tray with BD¿Quincke Needle recalled by Becton Dickinson &Becton DickinsonProcessing DeviationNationwide
DeviceCLASS IBD¿Spinal Tray with BD¿Whitacre Needle recalled by Becton Dickinson &Becton DickinsonProcessing DeviationNationwide
DeviceCLASS IBD¿Spinal Tray with BD¿Whitacre Needle, BD¿Quincke Needle recalledBecton DickinsonProcessing DeviationNationwide
DeviceCLASS IBD¿Spinal Tray with BD¿Quincke Needle recalled by Becton Dickinson &Becton DickinsonProcessing DeviationNationwide
DeviceCLASS IBD¿Spinal Tray with BD¿Whitacre Needle recalled by Becton Dickinson &Becton DickinsonProcessing DeviationNationwide
DeviceCLASS IBD¿Spinal Tray with BD¿Whitacre Needle recalled by Becton Dickinson &Becton DickinsonProcessing DeviationNationwide
DeviceCLASS IBD¿Spinal Tray with BD¿Quincke Needle recalled by Becton Dickinson &Becton DickinsonProcessing DeviationNationwide
DeviceCLASS IBD¿Spinal Tray with BD¿Whitacre Needle recalled by Becton Dickinson &Becton DickinsonProcessing DeviationNationwide
DeviceCLASS IISwan-Ganz Catheter recalled by Becton, Dickinson andBecton DickinsonPackaging DefectsNationwide
DeviceCLASS IISwan-Ganz Pacing Catheter recalled by Becton, Dickinson andBecton DickinsonPackaging DefectsNationwide
DeviceCLASS IISwan-Ganz Jr Catheter recalled by Becton, Dickinson andBecton DickinsonPackaging DefectsNationwide
DeviceCLASS IIBD GasPak EZ Campy Pouch System recalled by Becton Dickinson &Becton DickinsonOtherNationwide
DeviceCLASS IIBD GasPak EZ CO2 Pouch System recalled by Becton Dickinson &Becton DickinsonOtherNationwide
DeviceCLASS IINon-Sterile BD Luer-Lok Tip Syringe Only recalled by Becton Dickinson &Becton DickinsonPackaging DefectsNationwide
DeviceCLASS IIBD Luer Tip Caps recalled by Becton Dickinson &Becton DickinsonOtherNationwide
DeviceCLASS IIBD Kiestra" Isolate Suspension Cuvette Array recalledBecton DickinsonOtherNationwide
DeviceCLASS IIBD Phoenix M50 Instrument, labeled as the following recalledBecton DickinsonOtherNationwide
DeviceCLASS IIBD MAX System, for in vitro diagnostic (IVD) use recalledBecton DickinsonOtherNationwide
DeviceCLASS IIBD Bactec Blood Culture System, labeled as the following recalledBecton DickinsonPackaging DefectsNationwide
DeviceCLASS IIBD Veritor Connect recalled by Becton Dickinson &Becton DickinsonDevice MalfunctionNationwide
DeviceCLASS IIBD Bactec Blood Culture System, labeled as the following recalledBecton DickinsonOtherNationwide
DeviceCLASS IIBD EpiCenter Microbiology Data Management System recalledBecton DickinsonOtherNationwide
DeviceCLASS IIBD COR System recalled by Becton Dickinson &Becton DickinsonDevice MalfunctionNationwide
DeviceCLASS IIBD Bactec Mgit 960 Pza Kit recalled by Becton Dickinson &Becton DickinsonSterilityNationwide
DeviceCLASS IIBD BBL TB Stain Kit recalled by Becton Dickinson &Becton DickinsonOther14 states
DeviceCLASS IIBD PCR Cartridges used with MAX System recalled by Becton Dickinson &Becton DickinsonOtherNationwide
DeviceCLASS IIBD Phoenix M50 Automated Microbiology System recalledBecton DickinsonOtherNationwide
DeviceCLASS IIBactec 9120 System recalled by Becton Dickinson &Becton DickinsonOtherNationwide

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.