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B. Braun Medical, Inc.

B. Braun Medical, Inc. Recalls

All product recalls associated with B. Braun Medical, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

Most Recent

Jan 2026

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 17401–17420 of 21320 recalls

B. Braun Medical, Inc.: Outlook Safety Infusion System IV Set with Universal Spik...

Device defect is occlusion/no flow.

FDAMar 27, 2009Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Ultrasite ADDitIV Primary IV Set with Universal Spike, Ba...

Device defect is occlusion/no flow.

FDAMar 27, 2009Nationwide• B. Braun Medical, Inc.

Radiometer America Inc: Reference Electrode Membranes for use with blood gas anal...

Analysis of customer data, (for ABL 8X7 customers) has shown that the reference membranes are out of analytical specifications when replaced as specified in the device labeling. These errors in analytical specifications could lead to inadequate or clinical interventions (therapy) or misleading interpretation of patient status in clinical settings.

FDA

1...869 870871872 873...1066

Page 871 of 1066Next

Mar 26, 2009

CT, FL, GA +14 more

• Radiometer America Inc

Funnel Pre-Filters (Outerwears Inc.) – Fire Hazard (2009)

Fire/Burn Risk

These filters are used to fuel-up off-road and racing vehicles. The recall involves Outerwears Funnel Pre-Filters, or fuel funnel pre-filters, with the model numbers 20-2465-03, 20-2466-03, 20-2467-03, and 20-2474-03. The red fabric mesh filters were available in two sizes, small and large, and in two different shapes to accommodate various sizes of fueling funnels. The name of the manufacturer, Outerwears, is the only marking on the product.

CPSCMar 26, 2009Nationwide• Outerwears Inc., of Schoolcraft, Mich.

American Optisurgical Inc: American Optisurgical, Horizon Phacoemulsification System...

Device operation interrupted: A software bug causes Phaco to stop when vacuum goes above 300 mmHg while in Multi Burst mode. Use of this product at the parameters specified above could lead to a delay in surgery that might present a health risk.

FDAMar 24, 2009CA• American Optisurgical Inc

St. Jude Medical: EP-4 Computerized Cardiac Stimulator; SJM Part Numbers: 0...

Non-compliance with IEC Standard 60601-1 Clause 57.6 relative to fusing of AC input line. The neutral line is not fused. The hot line in fused. Clause 57.6 calls for both lines to be fused.

FDAMar 23, 2009Nationwide• St. Jude Medical

Boston Scientific CRM Corp: Boston Scientific COGNIS CRT-D, Cardiac Resynchronization...

Lead connection issues or fracture increases probability of inappropriate therapy: Inappropriate shocks, inappropriate anti-tachycardia pacing therapy, or inappropriate inhibition of needed bradycardia pacing therapy.

FDAMar 23, 2009PR• Boston Scientific CRM Corp

Medtronic Cardiovascular Revascularization & Surgical Therap: Medtronic Ideal MAXPAC Total System, Catalog Numbers: TS1...

Medtronic has identified a small number of One Source Kits and MAXPAC/Total System lots with incorrect Use Before Dates on the outer kit package label. The Use Before Date on the outer label of the kit/pack does not accurately reflect the Use Before Date of the components within the kit/pack. For affected product, the outer label lists a date which exceeds the earliest Use Before Date of the com

FDAMar 23, 2009AZ, CA, CO +20 more• Medtronic Cardiovascular Revascularization & Surgical Therap

Boston Scientific CRM Corp: Boston Scientific TELIGEN, Implantable Cardiac Defibrilla...

FDAMar 23, 2009PR• Boston Scientific CRM Corp

Medtronic Cardiovascular Revascularization & Surgical Therap: Medtronic One Source Pack Magellan, Catalog Number: COS31...

FDAMar 23, 2009AZ, CA, CO +20 more• Medtronic Cardiovascular Revascularization & Surgical Therap

Medtronic Neuromodulation: Medtronic N'Vision 8870 Application Card for use in the M...

Routine monitoring of Medtronic's vigilance program identified user related programming errors. Medtronic has received reports of both overdose and underdose that were the result of programming use of SynchroMed implantable infusion pumps. These errors were most commonly associated with: --Priming Bolus Programming; and --Bridge Bolus Programming. Pump programming errors that result in overdos

FDAMar 23, 2009Nationwide• Medtronic Neuromodulation

Medtronic Cardiovascular Revascularization & Surgical Therap: Medtronic One Source Pack, Catalog Numbers: ATLS21, ATLS2...

FDAMar 23, 2009AZ, CA, CO +20 more• Medtronic Cardiovascular Revascularization & Surgical Therap

Siemens Medical Solutions USA, Inc.: Auxiliary 2 MHz Continuous Wave (CW) transducer, model nu...

Fire/Burn Risk

Overheating. A software bug may cause the transducer to overheat when used with certain transducer models. The transducer can become noticeably hot within a few minutes, which may cause patient discomfort or burns.

FDAMar 21, 2009Nationwide• Siemens Medical Solutions USA, Inc.

Biomet Microfixation, Inc.: Lactosorb Pectus Stabilizer, model number: 01-3805. Distr...

This recall is based on the occurrence of known adverse effects identified in the device instructions for use. Bending, fracture, loosening, rubbing and migration of the devices can occur as a result of excessive activity, trauma or load bearing. Implantation of foreign materials can result in an inflammatory response or allergic reaction.

FDAMar 20, 2009AL, AZ, CA +25 more• Biomet Microfixation, Inc.

Siemens Medical Solutions USA, Inc.: Siemens Medical Solutions USA, Inc., ACUSON AcuNav ultra...

Screen Image Quality. An assembly issue on SwiftLink connectors may cause reduced/degraded image quality when using ACUSON AcuNav ultrasound catheter transducers.

FDAMar 20, 2009IN• Siemens Medical Solutions USA, Inc.

Boston Scientific Corporation: Boston Scientific, Flexima and Percuflex Drainage Cathete...

Boston Scientific Corporation is initiating an urgent Field Correction related to its Flexima and Percuflex Drainage Catheter Family (Pigtail Style). During the attempted removal of the device, sutures were separated from the catheter and remained in the patient.

FDAMar 18, 2009DC, PR• Boston Scientific Corporation

Solar System DNA Kits (FloraCraft) – Lead Paint Issue (2009)

This recall involves the "Solar System" and the "DNA" children's educational craft kits sold under the FloraCraft and HYGLOSS brand names. The kits contain green coated wires that measure 14 ½ inches long and Styrofoam shapes. The following model numbers are included in this recall. The model number is located on the kit's packaging. Craft Kits Model Number Solar System Kit SS2003 SS101 59901 SS2003P DNA Kit DNA2003 59903 DNA2003P

CPSCMar 18, 2009Nationwide• FloraCraft Corp., of Ludington, Mich.

Zero Turn Riding Mowers (Kubota) – Fire Risk (2009)

Fire/Burn Risk

The recalled riding mowers are propelled by gasoline V-twin engines and have 48-inch, 54-inch or 60-inch wide mower decks. The mowers come with adjustable roll bars and have 22 or 27 horsepower engines and are bright orange with KUBOTA decals on both sides behind the driver's seat. This recall includes the following model numbers: ZG222(serial numbers 10002 through 13673), ZG227 (serial numbers 10002 through 12957), ZG327 (serial numbers 10004 through 13318) which can be identified by the model designation and serial number on the data plate located on the right side frame, either before the mower deck or immediately after the mower deck.

CPSCMar 17, 2009Nationwide• Kubota Manufacturing of America Corp., of Gainesville, Ga.

Neuronetics, Inc.: NeuroStar TMS Therapy System/SenStar Treatment Link. The...

Fire/Burn Risk

SenStar Treatment Link may have an open circuit that during use with the NeuroStar TMS Therapy system may cause arcing and heat damage to the SenStar and/or treatment coil. Heating of the SenStar during use has a potential risk of minor scalp burn to patients.

FDAMar 16, 2009Nationwide• Neuronetics, Inc.

Spectranetics Corporation: Spectranetics SLS II Laser Sheath Kit, 14F, REF 500-012, ...

Catheter outer jacket may split during use.

FDAMar 16, 2009Nationwide• Spectranetics Corporation