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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)

127

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 22661–22680 of 25000 recalls

B. Braun Medical, Inc.: Adult Metriset w/Cassette 2 inj sites, LL 120 in. Item/Ca...

incorrect burette was packaged with the product

FDAJun 30, 2008Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Burette Set w/150 ml Burette w/15 um filter & Ultrasite i...

incorrect burette was packaged with the product

FDAJun 30, 2008Nationwide• B. Braun Medical, Inc.

Acrymed Incorporated: ON-Q Silver Dressing is a Antimicrobial wound dressing co...

The Silver Dressing, lot H0705J and H0706J may contain dressings that are not properly sealed in the foil pouch, which could affect sterility of the dressing.

FDAJun 30, 2008Nationwide

1...1132 113311341135 1136...1250

Page 1134 of 1250Next

• Acrymed Incorporated

RXV Golf Cars (E-Z-GO) – Fall Hazard (2008)

This recall involves electric and gasoline-powered Fleet RXV, Freedom RXV and RXV Shuttle 2+2 golf cars. The model names and the E-Z-GO logo are printed on the sides and front panel of all three vehicles. Serial numbers ranging from 9300001 to 9300188 and 5000000 to 5021328 are printed on a plate attached to the steering column, and the front and rear frames.

CPSCJun 27, 2008Nationwide• E-Z-GO, of Augusta, Ga. (a Textron Company)

Philips Medical Systems North America Co. Phillips: Motorized Height Ceiling Suspensions (MCS) and motorized ...

Monitor ceiling carriage may separate from the monitor ceiling suspension.

FDAJun 26, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Starion Instruments: Starion Instruments Real Hand ThermaSeal Thermal Ligating...

Due to an improper fixture revision, device may be missing a screw at the jaw assembly, resulting in jaw components falling off during use.

FDAJun 26, 2008Nationwide• Starion Instruments

2nd Nature Cribs (Stanley Furniture) – Entrapment Risk (2008)

This recall involves the full size 2nd Nature Built to Grow cribs, model number 353-14-220. Model and serial numbers are located on the headboard. The crib is natural maple in color. Only the following serial numbers are included in the recall: 353-14-220-L-01, 353-14-220-L-02, 353-14-220-L-03, 353-14-220-L-04, 353-14-220-L-05, 353-14-220-L-06, 353-14-220-L-07, 353-14-220-L-08, 353-14-220-L-101, and 353-14-220-L-103. The recall does not include cribs sold after December 2007.

CPSCJun 26, 2008Nationwide• Stanley Furniture Company Inc., of Stanleytown, Va.

Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa: Applied Medical, Separator Abdominal Access System REF: C...

Potential inability to insufflate through the stopcock. Under certain circumstances, a flexible elastomeric component inside the 15mm trocar can stretch into a configuration that blocks the flow of insufflation gas (C02).

FDAJun 25, 2008Nationwide• Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa

Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa: Applied Medical, Lap Banding Kit, REF: K0398 Contains: ...

FDAJun 25, 2008Nationwide• Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa

Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa: Applied Medical, Lap Roux-EN-Y Kit, REF: K2129 Contains...

FDAJun 25, 2008Nationwide• Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa

Gyrus ACMI Corporation: Gyrus ACMI 10 Fr. Dual Lumen Catheter Reference Number: 6...

Particulate matter in the catheter

FDAJun 25, 2008Nationwide• Gyrus ACMI Corporation

CAS Medical Systems, Inc.: 740 Series Multiparameter Monitor Software Version 3.0 Mo...

Software: Audible alarm may be silenced if changed from the factory setting

FDAJun 24, 2008Nationwide• CAS Medical Systems, Inc.

Playground Tire Swings (Miracle Recreation) – fall hazard (2008)

The recalled Tire Swing consists of a tire, which hangs from a swivel and three chains. The recall includes the following products and model numbers: Kids' Choice Arch Tire Swing Sets Model # 714-852 Kids' Choice Arch Tire Swing Extension Model # 714-852-X Kids' Choice Arch Tire Swing Swivel Replacement Model #278

CPSCJun 24, 2008Nationwide• Miracle Recreation Equipment Co., of Monett, Mo.

Water Pump Motors (A.O. Smith) – fire hazard (2008)

Fire/Burn Risk

The recall involves motors included with lawn sprinkler pumps and jet pumps manufactured by F. E. Myers Co. The recall also includes replacement pump motors that were sold separately. Model Number Product Description QP10 Lawn Sprinkler Pump QP10B Lawn Sprinkler Pump with Brass Impeller HJ100S Shallow Well Jet Pump HJ100S-1 Shallow Well Jet Pump with Brass Impeller HJ100D Deep Well Jet Pump HJ100D-LR Deep Well Jet Pump Less Regulator HJ100D-1 Deep Well Jet Pump with Brass Impeller 20935A000K Individually Sold Replacement Motor Only pumps manufactured between August 2007 and May 2008 are included in the recall. The pump's model number, manufacturing date code and the name "Myers" can be located on the pump's nameplate and packaging. The pump's motor has "A. O. Smith" and model number "C48D52B86" on the motor's nameplate. The replacement motor's packaging has "Myers" and model number "20935A000K" printed on it. Products with an "OK" sticker on the product or packaging are not included in the recall.

CPSCJun 24, 2008Nationwide• A.O. Smith Electrical Products Co., of Tipp City, Ohio

Philips And Neusoft Medical Systems Co., Ltd.: NeuViz Dual series computed Tomography Scanner System, X-...

Potential for R-host box and components inside to be detached of its mounting during the gantry rotor rotation. There is a potential for components to be damaged inside the system gantry and for the internal components to be expelled from the system gantry and injure the patient, operator, bystander or service people.

FDAJun 23, 2008CO, FL, IN +5 more• Philips And Neusoft Medical Systems Co., Ltd.

StatSpin, Inc., dba Iris Sample Processing: StatSampler 200 uL, Li Heparin (micro blood collector) Re...

EDTA inadvertently mixed with lithium heparin solution contained in capillary tubes.

FDAJun 20, 2008CA, CO, FL +7 more• StatSpin, Inc., dba Iris Sample Processing

Orthosoft, Inc. dba Zimmer CAS: Navitrack System - OS Knee Universal, Orthopedic Stereota...

ZIMMER CAS voluntarily conducted a retrospective recall of the Navitrack System - OS Knee Universal, due to software anomalies which were corrected with a new revision in version 2.2.1.3.

FDAJun 20, 2008CA, FL, GA +17 more• Orthosoft, Inc. dba Zimmer CAS

Datex Ohmeda, Inc. dba GE Healthcare: Giraffe OmniBed, labeled in part: ***GE Healthcare 8880...

Manufacturer of neonatal incubators changed the device labeling to account for new use and care instructions.

FDAJun 20, 2008Nationwide• Datex Ohmeda, Inc. dba GE Healthcare

Orthosoft, Inc. dba Zimmer CAS: Navitrack¿ System - OS Knee Universal, Orthopedic Stereot...

ZIMMER CAS voluntarily conducted a retrospective recall of the Navitrack System - OS Knee Universal, due to software anomalies which were corrected with a new revision in version 2.2.1.3.

Class IIILow

FDAJun 20, 2008CA, FL, GA +17 more• Orthosoft, Inc. dba Zimmer CAS

Intraop Medical Corporation: Mobetron Model 1000, mobile electron linear accelerator, ...

Docking screw/nut failure, which may result in a treatment head dropping, potentially impacting the patient.

FDAJun 20, 2008Nationwide• Intraop Medical Corporation