B Braun Medical recalls

B Braun Medical has 447 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 16 Sep 2026. 240 are still ongoing. 158 were reported in the last 12 months.

Total recalls447since 2012
Last 12 months158reported
Class I4510% of total
Ongoing240latest 16 Sep 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 45 10%Class II 401 90%Class III 1 0%

By year

Ongoing b braun medical recalls

240 active

All b braun medical recalls, newest first

447 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS I0.9% Sodium Chloride Injection, USP Partial Fill recalledSodium ChlorideB Braun MedicalParticulate MatterNationwide
DeviceCLASS IIExtension Set Discofix Four Way Stopcock recalled by B Braun MedicalB Braun MedicalOtherNationwide
DrugCLASS ILactated Ringer's Injection USP Excel container recalledLactated RingersB Braun MedicalParticulate MatterNationwide
DeviceCLASS IDesign Options Spinal Tray Spinal Needle Anesthesia recalledB Braun MedicalProcessing DeviationNationwide
DeviceCLASS IISesk Upmc Double Catheter Tray recalled by B Braun MedicalB Braun MedicalDevice MalfunctionNationwide
DeviceCLASS IICesk Riverside Health System recalled by B Braun MedicalB Braun MedicalDevice MalfunctionNationwide
DeviceCLASS IILyndon B Johnson Hospital Spinal Epid recalled by B Braun MedicalB Braun MedicalDevice MalfunctionNationwide
DeviceCLASS ISpinal Needle procedure kits: Material Description (Material Number) recalledB Braun MedicalProcessing DeviationNationwide
DeviceCLASS IIBpsk, Blockjocks Tray recalled by B Braun MedicalB Braun MedicalDevice MalfunctionNationwide
DeviceCLASS IINes1725kfxl Spinal Epid Closed Tip Cath recalled by B Braun MedicalB Braun MedicalDevice MalfunctionNationwide
DeviceCLASS IICesk Shands Jacksonville recalled by B Braun MedicalB Braun MedicalDevice MalfunctionNationwide
DeviceCLASS IICesk Northside Anesthesia Tray recalled by B Braun MedicalB Braun MedicalDevice MalfunctionNationwide
DeviceCLASS ISpinocan Spinal Needle procedure kits: Material Description recalledB Braun MedicalProcessing DeviationNationwide
DeviceCLASS IICesk Harris Methodist recalled by B Braun MedicalB Braun MedicalDevice MalfunctionNationwide
DrugCLASS ILactated Ringer's Injection USP container recalled by B Braun MedicalLactated RingersB Braun MedicalParticulate MatterNationwide
DrugCLASS IISterile Water for Injection recalled by B Braun MedicalSterile WaterB Braun MedicalSterilityNationwide
DrugCLASS II0.9 % Sodium Chloride Irrigation recalled by B Braun MedicalSodium Chloride For IrrigationB Braun MedicalSterilityNationwide
DrugCLASS IILactated Ringer's Irrigation, Sterile, Ex only recalledLactated Ringers IrrigationB Braun MedicalSterilityNationwide
DrugCLASS IIDextrose Injection recalled by B Braun MedicalDextroseB Braun MedicalSterilityNationwide
DeviceCLASS IB. Braun Hemodialysis Bloodlines recalled by B Braun MedicalB Braun MedicalOtherNationwide
DeviceCLASS IB. Braun Hemodialysis Bloodlines, Low Vol, NO Chamber Pump Segment recalledB Braun MedicalOtherNationwide
DeviceCLASS IB Braun Hemodialysis Bloodlines, Low Vol, NO Chamber Pump Segment recalledB Braun MedicalOtherNationwide
DeviceCLASS IB. Braun Hemodialysis Bloodlines, Streamline Fresenius For Davita recalledB Braun MedicalOtherNationwide
DeviceCLASS IB. Braun Hemodialysis Bloodlines recalled by B Braun MedicalB Braun MedicalOtherNationwide
DeviceCLASS IB. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long recalledB Braun MedicalOtherNationwide
DeviceCLASS IIBBraun Medical Winged INF recalledB Braun MedicalDevice MalfunctionNationwide
DeviceCLASS IIB. Braun Winged Infusion, Single PK recalled by B Braun MedicalB Braun MedicalDevice MalfunctionNationwide
DeviceCLASS IIB. Braun Winged INF SET recalled by B Braun MedicalB Braun MedicalDevice MalfunctionNationwide
DeviceCLASS IIOutlook set utilized in gravity IV administration sets recalledB Braun MedicalOtherPA
DeviceCLASS IIIV Administration Set utilized recalled by B Braun MedicalB Braun MedicalOtherPA

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.