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 141–160 of 263 recalls

B. Braun Medical, Inc.: CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189

The filter capacity is not achieved due to damage of the filter membrane.

FDAJul 10, 2019AL, CA, FL +7 more• B. Braun Medical, Inc.

B. Braun Medical, Inc.: CE17TKFCSN CON EPI TRAY W/17G TUHY NRFIT Catalog # 339187

The filter capacity is not achieved due to damage of the filter membrane.

FDAJul 10, 2019AL, CA, FL +7 more• B. Braun Medical, Inc.

B. Braun Medical, Inc.: CE18TKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339188

The filter capacity is not achieved due to damage of the filter membrane.

FDAJul 10, 2019AL, CA, FL +7 more• B. Braun Medical, Inc.

1...6 789 10...14

Page 8 of 14Next

B. Braun Medical, Inc.: ES1827KN SPINAL/EPIDURAL TRAY NRFIT Catalog # 339115

The filter capacity is not achieved due to damage of the filter membrane.

FDAJul 10, 2019AL, CA, FL +7 more• B. Braun Medical, Inc.

B. Braun Medical, Inc.: ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114

The filter capacity is not achieved due to damage of the filter membrane.

FDAJul 10, 2019AL, CA, FL +7 more• B. Braun Medical, Inc.

Heparin Sodium (B. Braun Medical) – subpotent drug (2019)

Subpotent Drug: low out-of-specification results were identified for the drug anti-factor IIa potency which is intended to ensure that the potency of heparin is within the USP specifications.

Class IIModerate

FDAJun 13, 2019Nationwide• B. Braun Medical Inc

B. Braun Medical, Inc.: B.Braun Infusomat Space Volumetric Infusion Pump Administ...

Potential for the Infusion Pump Administration Set to leak and/or disconnect at the bonded joint between the tubing and Injection Site (Y-Site).

FDAMay 1, 2019TX• B. Braun Medical, Inc.

2012 BRAUNABILITY DODGE WHEELCHAIR VAN Recall: ELECTRONIC STABILITY CONTROL (ESC)

On July 20, 2018 Braun Corporation (Braun) filed a recall for certain 2017-2018 BraunAbility Dodge Side Entry Vans with a manual in-floor wheelchair ramp built on Dodge RT minivan chassis. The brake lines may not be connected to the corresponding ports on the hydraulic control unit, causing reduced performance of the electronic stability control (ESC) system. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 135, "Light Vehicle Brake Systems," and 126, "Electronic Stability Control Systems." On August 21, 2018, Braun expanded this recall to include an additional 31,165 vehicles. Included in this update are 2012-2016 BraunAbility Dodge Side Entry Vans and 2012-2018 Chrysler Town and Country Side Entry Vans.

NHTSAJul 20, 2018Nationwide• BRAUNABILITY

Sodium Chloride Irrigation (B. Braun) – Particulate Matter (2018)

Presence of Particulate Matter: Customer complaint of particulate matter which has been identified as polyethylene, which is consistent with the material used to manufacture the container cap was received.

Class IIModerate

FDAFeb 16, 2018Nationwide• B. Braun Medical Inc

Acetic Acid Irrigation (B. Braun) – Particulate Matter (2017)

Presence of Particulate Matter: identified as polyethylene, which is consistent with the material used to manufacture the contain cap

Class IIModerate

FDADec 15, 2017Nationwide• B. Braun Medical Inc

2016 BRAUN BRAUNABILITY MXV Recall: SEATS

Braun Corporation (Braun) is recalling certain model year 2016 BraunAbility MXV wheelchair accessible conversion vehicles built on Ford Explorer chassis. If the driver or front passenger seat is moved to its most rearward position, the seat position sensor may be dislodged, preventing the air bag control unit from accurately calculating the frontal air bag deployment force needed in the event of a crash.

NHTSAOct 3, 2017Nationwide• BRAUN

2016 BRAUN MXV Recall: EQUIPMENT ADAPTIVE/MOBILITY

Braun Corporation (Braun) is recalling certain model year 2016 MXV vehicles manufactured February 8, 2016, to June 23, 2016 and built on a Ford Explorer chassis. The passenger seat electrical harness may be incorrectly routed and can be crushed between the seat structure and the seat riser manufactured as part of the wheelchair accessible conversion.

NHTSAJul 26, 2016Nationwide• BRAUN

Dextrose Injection (B. Braun) – Fungal Contamination (2016)

Non-Sterility: fungal contamination due to leaking containers.

FDAMar 25, 2016Nationwide• B. Braun Medical Inc

2014 BRAUN MODIFIED CHRYSLER Recall: EQUIPMENT:OTHER:LABELS

Braun Corporation (Braun) is recalling certain model year 2013-2015 Braun-modified Chrysler and Dodge vehicles manufactured December 19, 2012, to May 5, 2015. The affected vehicles have certification labels that may have incorrect gross vehicle weight rating (GVWR) information, and front and rear gross axle weight rating (GAWR) information printed on the Certification labels. As such, these vehicles fail to comply with the requirements of 49 CFR Part 567, "Certification."

NHTSAJun 15, 2015Nationwide• BRAUN

B. Braun Medical, Inc.: B.Braun Accuflo 100ML/H 100ML Elastomeric Infusion Device...

The primary packaging label (inner pouch label) indicates that the package contents are Catalog Item: CT-1000-250, while the secondary packaging label (outer carton label) indicates the contents are CT-1000-100. The actual contents are a CT-1000-100.

Class IIModerate

FDAAug 6, 2014IN, MO• B. Braun Medical, Inc.

Sodium Chloride Injection (B. Braun) – Incorrect Bar Code (2013)

Labeling: Wrong Bar Code; Bar code scans as 0.15% Potassium Chloride in 0.9% Sodium Chloride (20 mEq K/liter).

Class IIModerate

FDANov 27, 2013Nationwide• B. Braun Medical Inc

FreAmine HBC 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

ProcalAmine 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

Ceftriaxone 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