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The Braun Corporation

The Braun Corporation Recalls

All product recalls associated with The Braun Corporation.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 33661–33680 of 37665 recalls

The Braun Corporation: Braun wheelchair lift, model NVL, Braun Corporation, Win...

The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured.

FDAAug 15, 2007Nationwide• The Braun Corporation

Classic Beauty Rest Electric Throws – Safety Issue (2007)

Fire/Burn Risk

This recall involves 52 inch by 62 inch electric warming throws. The 100% acrylic throws were sold in various colors and patterns and have model number BST-06-THR. The model number is located on the care label sewn into the throw. "Classic Beautyrest" and "Automatic Electric Warming Throw" is printed on the product's packaging. Model numbers with the following date codes are included in this recall: B00106 through B36506. Bilt-Safe Technologies, Inc. and the date code are printed on the bottom of the care label.

CPSCAug 15, 2007Nationwide• Ningbo Veken Elite International Trading Company Ltd., of China

The Braun Corporation: Braun wheelchair lift, model NCL, Braun Corporation, Win...

1...1682 168316841685 1686...1884

Page 1684 of 1884Next

The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured.

FDAAug 15, 2007Nationwide• The Braun Corporation

Merit Medical Systems, Inc: Merit Medical Surgical Convenience Kits, Custom and SPPT,...

Expiration Dating; Some Convenience Kits contain medications and/or skin preparations that may expire before the expiration date on the outer package label.

FDAAug 15, 2007Nationwide• Merit Medical Systems, Inc

Smiths Medical MD, Inc.: Smiths Medical CADD-Sentry Pro Medication Safety Software...

Incorrect dosage possible: A software anomaly in the CADD-Sentry Pro Administrator software (version B) where the values of a weight based protocol go to zero or round up to the next higher hundredths place, even if Administrator displayed the values correctly at data entry.

FDAAug 14, 2007CO, MD, UT• Smiths Medical MD, Inc.

GE Healthcare: GE Definium 8000 , model 5135678, Digital Radiographic Sy...

Necessary certification labels are missing from the x-ray contol.

FDAAug 13, 2007Nationwide• GE Healthcare

GE Healthcare: GE Precision 500D, model 2403790-3, Radiographic and Fluo...

Necessary certification labels are missing from the x-ray contol.

FDAAug 13, 2007Nationwide• GE Healthcare

C.R. Bard Access Systems, Inc: Guidewire, 70cm x 1mm, REF 5583705, Sterile, Single Use, ...

Metal guidewires used in Hemodialysis Catheters may have been reverse loaded within the dispenser. Potential exists for the stiff end of the guidewire to be inserted into the patient instead of the flexible end.

FDAAug 10, 2007Nationwide• C.R. Bard Access Systems, Inc

Summit Industries Inc.: PCS125 Swivel Collimator, Model F100; Manual Radiographic...

The F100 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table.

FDAAug 10, 2007Nationwide• Summit Industries Inc.

Summit Industries Inc.: LX125V Swivel Collimator, Model E600; Manual Radiographic...

The E600 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table.

FDAAug 10, 2007Nationwide• Summit Industries Inc.

Summit Industries Inc.: LX125 Swivel Collimator, Model D800; Manual Radiographic ...

The D800 Swivel Collimator may come loose from the tubestand and fall onto the x-ray table.

FDAAug 10, 2007Nationwide• Summit Industries Inc.

Abbott Laboratories Inc.: Abbott Clinical Chemistry Aeroset/Architect (c Systems)Bi...

Incorrect Calibrator values: changes in a raw material used in the Bilirubin Calibrator value assignment process contributed to variability in the preparation of the standard.

FDAAug 10, 2007PR• Abbott Laboratories Inc.

Linvatec Corp.: ConMed Linvatec, Ultrapower Burs, Linvatec Corporation, L...

Compromised sterility: ConMed Linvatec medical devices packaged within a certain Peel Pouch Sterile Package may have compromised sterility due to an improper seal.

FDAAug 9, 2007Nationwide• Linvatec Corp.

Toshiba Notebook Battery (Sony) – fire risk (2007)

Fire/Burn Risk

The recalled lithium-ion batteries were sold with, or sold separately to be used with, the following notebook computer models: Satellite A100, Satellite A105 and Tecra A7. The battery model is printed on the battery. Model Computer Model Prefix Number (first 2 digits of serial number) Model Prefix (first 6 characters) Manufacturing Date Range Estimated Retail Pricing (when sold) Satellite A100 16, 26, 36, 46 PSAA0U January 1, 2006 - April 30, 2006 About $1,300 Satellite A105 16, 26, 36, 46 PSAA2U PSAA8U PSAA9U January 1, 2006 - April 30, 2006 About $1,000 Tecra A7 16, 26, 36, 46 PTA70U PTA71U January 1, 2006 - April 30, 2006 About $700

CPSCAug 9, 2007Nationwide• Sony Energy Devices Corp., of Japan (battery cells)

Garden Treasures Cloud 9 Chair (Taizhou Yongjiang) – fall hazard (2007)

This recall involves the Garden Treasures Cloud 9 Beyond outdoor lounge chairs. The chairs are tan in color, have a light steel frame, cloth seat, a pillow at the headrest and an adjustable sun visor.

CPSCAug 9, 2007Nationwide• Taizhou Yongjiang Arts and Crafts Collective Ltd., of China

VNUS Medical Technologies Inc: VNUS 7F ClosureFAST Catheter, Order #: CF7-7-60 (60 cm wo...

Instructions for Use change: Instructions for Use have been changed to include a modified placement recommendation.

FDAAug 8, 2007Nationwide• VNUS Medical Technologies Inc

BD Diagnostic Systems Lee Laboratories: DIFCO Laboratories, FA Streptococcus Group A, 5mL, Catal...

Incorrect result: The product exhibited decreased fluorescence when testing with the homologous control organism.

FDAAug 8, 2007Nationwide• BD Diagnostic Systems Lee Laboratories

E Light (Plan 9) – fire hazard (2007)

Fire/Burn Risk

The E Light is a 12-Volt DC light fixture with recessed LEDs typically mounted on the ceiling or under a counter. The recalled light is a flat, white rectangle with three LEDs (in the three-watt model) or six LEDs (in the six-watt model).

CPSCAug 3, 2007Nationwide• Plan 9 Inc., of White Salmon, Wash.

Medtronic Neuromodulation: Medtronic SynchroMed EL Programmable Pump, Model 8626-10....

Pump motor stall due to gear shaft wear

FDAAug 3, 2007AL, AK, AZ +49 more• Medtronic Neuromodulation

Raleigh Cadent Bicycle (Carbonage) – fork break risk (2007)

The recall involves the 2007 Raleigh Cadent 1.0, Cadent 2.0 and Cadent Carbon bicycle models with carbon forks. "Raleigh" is printed on the down tube of the bicycle, and the model name is printed on the top tube.

CPSCAug 3, 2007Nationwide• Carbonage Technology, of Baoan, China