Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

Home
/
Brands
/
B. Braun Medical Inc

B. Braun Medical Inc Recalls

All product recalls associated with B. Braun Medical Inc.

Get alerts for this brand

Recall Summary

Total Recalls

263

Past Year

36

Class I (Serious)

18

Most Recent

Oct 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 161–180 of 263 recalls

Sodium Chloride Injection (B. Braun) – Particulate Matter Risk (2013)

Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.

FDANov 21, 2013Nationwide• B. Braun Medical Inc

Cefazolin Injection (B. Braun) – Particulate Matter Risk (2013)

Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.

FDANov 21, 2013Nationwide• B. Braun Medical Inc

TrophAmine Injection (B. Braun) – Particulate Matter Risk (2013)

Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.

1...7 8910 11...14

Page 9 of 14Next

Class IHigh

FDANov 21, 2013Nationwide• B. Braun Medical Inc

Cefazolin Injection (B. Braun) – Particulate Matter Risk (2013)

Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.

FDANov 21, 2013Nationwide• B. Braun Medical Inc

Sodium Chloride Injection (B. Braun) – Particulate Matter Risk (2013)

Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.

FDANov 21, 2013Nationwide• B. Braun Medical Inc

Hyperlyte CR Concentrate (B. Braun) – Particulate Matter Risk (2013)

Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.

FDANov 21, 2013Nationwide• B. Braun Medical Inc

Cefoxitin Injection (B. Braun) – Particulate Matter Risk (2013)

Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.

FDANov 21, 2013Nationwide• B. Braun Medical Inc

15% Amino Acids Injection (B. Braun) – Particulate Matter Risk (2013)

Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.

FDANov 21, 2013Nationwide• B. Braun Medical Inc

Cefepime and Dextrose Injection (B. Braun) – particulate matter (2013)

Presence of Particulate Matter: The 1g Cefepime for Injection USP and Dextrose Injection USP lot has been found to contain visible organic particulate matter in a reserve sample unit.

FDAOct 15, 2013Nationwide• B. Braun Medical Inc

2013 BRAUN VISION REAR ENTRY Recall: SUSPENSION:REAR

Braun is recalling certain model year 2008-2013 Vision Rear Entry mobility conversion vehicles built on Dodge and Chrysler minivan chassis from December 20, 2012, through March 21, 2013. The track bar mount assemblies were not properly welded during manufacturing. One or more welds are missing from the track bar which could result in separation from the rear axle.

NHTSAMar 25, 2013Nationwide• BRAUN

2013 BRAUN RAMPVAN Recall: VEHICLE SPEED CONTROL:ACCELERATOR PEDAL

Braun is recalling certain model year 2011-2013 Rampvan vehicles manufactured from May 8, 2012, through January 3, 2013. Braun Rampvans are Toyota Sienna minivans that have been modified for special use. The Braun-specific toe pan panel comes in close proximity to the accelerator pedal lever. There could be an interference of the toe panel pan and the accelerator pedal lever.

NHTSAJan 11, 2013Nationwide• BRAUN

2012 BRAUN ENTERVAN Recall: SEATS

Braun is recalling certain model year 2012 Entervan vehicles equipped with aftermarket seat covers, part numbers E51815K-D90-11 and E51817K-11, manufactured from February 28, 2012, through September 21, 2012. The seat covers may have been incorrectly installed with the driver seat cover on the passenger seat and vice versa and will have an 'SRS AIRBAG' label located on the inboard seat bolster.

NHTSAOct 9, 2012Nationwide• BRAUN

BRAUN VISTA-2 Equipment Recall: EQUIPMENT ADAPTIVE/MOBILITY

BRAUN IS RECALLING CERTAIN CENTURY-2 AND VISTA-2 WHEELCHAIR LIFTS MANUFACTURED FROM NOVEMBER 20, 2006, THROUGH SEPTEMBER 10, 2010, INSTALLED AS AFTERMARKET EQUIPMENT ON VARIOUS VANS AND TRANSIT BUSES. ON OCTOBER 8, 2012, BRAUN FILED AN AMENDED DEFECT INFORMATION REPORT TO INCLUDE MODEL YEAR 2008 THROUGH 2011 BRAUN-MODIFIED FORD E-350 PARATRANSIT VANS. OVER TIME AND WITH FREQUENT USE, THE ROLL STOP LATCHES ON THE OUTER BARRIER MAY BECOME BENT OR MISALIGNED.

NHTSAFeb 3, 2012Nationwide• BRAUN

2008 BRAUN TOWN & COUNTRY Recall: ELECTRICAL SYSTEM:WIRING

CHRYSLER IS RECALLING CERTAIN MODEL YEAR 2008 AND 2009 DODGE GRAND CARAVAN AND CHRYSLER TOWN & COUNTRY PASSENGER VEHICLES MANUFACTURED FROM FEBRUARY 2007 THROUGH SEPTEMBER 2009. SOME OF THE VEHICLES MAY HAVE BEEN BUILT WITH AN IMPROPERLY ROUTED WIRE HARNESS THAT MAY HAVE A CONDITION WHERE THE LOWER SLIDING DOOR HINGE BRACKET CAN MAKE CONTACT AND WEAR THROUGH THE WIRE INSULATION.

NHTSAJun 3, 2010Nationwide• BRAUN

2010 BRAUN TOWN AND COUNTRY Recall: FUEL SYSTEM, GASOLINE:STORAGE:TANK ASSEMBLY:FILLER PIPE AND CAP

THE BRAUN CORPORATION IS RECALLING CERTAIN MODEL YEAR 2008 THROUGH 2010 CHRYSLER TOWN & COUNTRY AND DODGE CARAVAN COMMERCIAL ENTERVANS WHICH WERE ALTERED BY BRAUN BETWEEN JANUARY 21, 2009 AND MARCH 19, 2010. DURING CONVERSION, THE CHASSIS WAS RAISED AND THE FLOOR WAS LOWERED TO ACCOMMODATE WHEELCHAIR ACCESSIBILITY FEATURES. IN RAISING THE CHASSIS, THE FUEL FILL PIPE COMES INTO CLOSER PROXIMITY TO THE LEFT REAR TIRE. IN ROUGH OR AGGRESSIVE DRIVING SITUATIONS, THE TIRE MAY INTERMITTENTLY CONTACT THE FUEL FILL PIPE.

NHTSAApr 13, 2010Nationwide• BRAUN

B. Braun Medical, Inc.: Outlook Pump IV Set w/Universal Spike, 2 Injection sites,...

System error 9 alarms. A System Error 9 alarm indicates a potential pressure loss in the pump cassette delivery chamber (chamber closest to the patient). This alarm is generated during the pumps initiation sequence and will not allow the set to be used. This requires a new set to be obtained, thus creating a potential for delay in therapy.

FDANov 24, 2009Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Outlook Pump Set w/150 ml Burette w/15um Filter & Safelin...

System error 9 alarms. A System Error 9 alarm indicates a potential pressure loss in the pump cassette delivery chamber (chamber closest to the patient). This alarm is generated during the pumps initiation sequence and will not allow the set to be used. This requires a new set to be obtained, thus creating a potential for delay in therapy.

FDANov 24, 2009Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Outlook Pump IV Set w/Universal Spike, 2 Safesite Inj sit...

System error 9 alarms. A System Error 9 alarm indicates a potential pressure loss in the pump cassette delivery chamber (chamber closest to the patient). This alarm is generated during the pumps initiation sequence and will not allow the set to be used. This requires a new set to be obtained, thus creating a potential for delay in therapy.

FDANov 24, 2009Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Outlook Pump IV Set w/Universal Spike & Spin Lock Connect...

System error 9 alarms. A System Error 9 alarm indicates a potential pressure loss in the pump cassette delivery chamber (chamber closest to the patient). This alarm is generated during the pumps initiation sequence and will not allow the set to be used. This requires a new set to be obtained, thus creating a potential for delay in therapy.

FDANov 24, 2009Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Outlook Pump IV Set w/Universal Spike Check Valve, 4 Ultr...

System error 9 alarms. A System Error 9 alarm indicates a potential pressure loss in the pump cassette delivery chamber (chamber closest to the patient). This alarm is generated during the pumps initiation sequence and will not allow the set to be used. This requires a new set to be obtained, thus creating a potential for delay in therapy.

FDANov 24, 2009Nationwide• B. Braun Medical, Inc.