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Compumedics Usa, Ltd

Compumedics Usa, Ltd Recalls

All product recalls associated with Compumedics Usa, Ltd.

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 16741–16760 of 17592 recalls

Compumedics Usa, Ltd: Compumedics E-Series Digital Amplifier System part number...

Fire/Burn Risk

Under specific conditions, the housing of the pulse oximeter contected to the amplifier can become excessively warm causing a burn upon contact with skin.

FDAFeb 24, 2005Nationwide• Compumedics Usa, Ltd

Proctor & Gamble Co: The product is a battery operated toothbrush. Spinbrush P...

The brushes may experience head breakage when insufficently rinsed after use and when used in combination with toothpastes containing a combination baking soda, peroxide, and sodium lauroyl sarcosinate.

FDAFeb 23, 2005Nationwide• Proctor & Gamble Co

Beckman Coulter Inc: Access Immunoasay Systems Digoxin Reagent

Variability in results on Patient and QC results of 20-25%, high and low.

1...836 837838839 840...880

Page 838 of 880Next

FDA

Feb 23, 2005

Nationwide

• Beckman Coulter Inc

Proctor & Gamble Co: The product is refill heads for battery powered toothbrus...

FDAFeb 23, 2005Nationwide• Proctor & Gamble Co

Built-in Dishwasher (GE) – Electrical Problem (2005)

Fire/Burn Risk

The following models are included in this recall and were sold after January 20, 2004: GE dishwasher models GSD5500G, GSD5560G, GSD5800G, GSD5900G, GSD5960G, EDW3000G, and EDW3060G, with serial numbers with the first letter A through T and the second letter G, or the serial letters VF. The serial number is important, as not all dishwashers with these model numbers are included in this recall. The model and serial number are located inside the door wall of the dishwasher.

CPSCFeb 18, 2005Nationwide• GE Consumer and Industrial of Louisville, Ky.

Rope Candle (Gardener's Supply) – Fire Hazard (2005)

Fire/Burn Risk

The Rope Candle is a 21-foot coiled beeswax candle that feeds up to a scissors-like vise. The candle is lit above the vise. The candle is 7 inches tall and sits on an antiqued copper-finish holder.

CPSCFeb 18, 2005Nationwide• Zhongshan Zhongnam Candle Manufacturer Co., Ltd. of China

Dentsply Friadent Ceramed: PepGen P-15 Putty (0.5cc)

PepGen P-15 Putty kit was labeled with the incorrect expiration date.

FDAFeb 17, 2005Nationwide• Dentsply Friadent Ceramed

Toddler Drinking Cup (Charles Products) – Safety Concern (2005)

The toddler cups are made of clear plastic with two handles and have a blue lid with a spout for young children to drink from. The dome-shaped container inside the cup contains blue and clear liquid, along with two toy dolphins, which appear to be swimming in the liquid. "MAUI OCEAN CENTER" is written on the side of the cups.

CPSCFeb 17, 2005Nationwide• Charles Products, of Bethesda, Md.

Philips Medical Systems Sales & Service Region No. America: Easy Access Image Management System with CL.Net.

Failure to update correctly when re-transmitting an image from the modality.

FDAFeb 16, 2005Nationwide• Philips Medical Systems Sales & Service Region No. America

Roche Molecular Systems Inc: TaqMan HBV Analyte Specific Reagent, Material Number 3322...

Low level of recombinant HIV DNA found in one lot of HBV QS which is a component of one lot of the TaqMan HBV ASR.

FDAFeb 14, 2005NC• Roche Molecular Systems Inc

Gas-Electric Heating Units (Trane/American Standard) – performance issue (2005)

Fire/Burn Risk

The recalled units include 2- through 5-ton Trane and American Standard heating and air conditioning packaged units. Affected units are combination gas heat and air conditioning systems installed outdoors only. Gas furnaces installed indoors are not included in this recall. The units have identification plates displaying the model number; serial number; and the year, month and day of manufacture. The plate is located on one end of the unit. The first four digits of all serial numbers indicate the year, fiscal week and day of manufacture. The recall includes: - All units with model numbers beginning with YCP or YCX and having serial numbers beginning with 3383 through 4475; - All units with model number beginning with YCY or YCZ and having serial numbers beginning with 4282 through 4475.

CPSCFeb 11, 2005Nationwide• Trane and American Standard, divisions of American Standard Inc., of Tyler, Texas

BISSELL Carpet Cleaner – handle defect (2005)

The recalled upright carpet deep cleaners have an open handgrip, a partially metal handle and come in a variety of colors. The word "BISSELL" is printed on the front of the unit. The recalled carpet cleaners have date codes beginning with 01, 02, 03 or 04 and include the following models: PowerLifter® Plus (model number 1620) PowerSteamer® ClearView® (model numbers 1692, 1692-1, 1692-R) Power Steamer® (model numbers 1685, 1693, 1693-R, 1693-W, 1694, 1694-1, 1694-R) Power Lifter® (model number 1694-3) Rubbermaid X-tra-Lift™ (model 9E00) The date codes and model numbers are printed on a label on the bottom of the unit. Cleaners with the model number and date codes listed above that are marked "Inspected" on or near the label are not included in the recall.

CPSCFeb 11, 2005Nationwide• BISSELL Homecare Inc., of Grand Rapids, Mich.

Philips Medical Systems Sales & Service Region No. America: Tomoscan

Potential for shift of reference lines.

FDAFeb 10, 2005Nationwide• Philips Medical Systems Sales & Service Region No. America

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo DR, model 7278 Single Chamber Implantabl...

Medtronic marquis family of ICD and CRT-D devices having batteries manufactured prior to December 2003 that may experience rapid battery depletion due to a specific internal battery short mechanism. Once a short occurs, depletion can take place within a few hours to a few days, after which there is a complete loss of device function.

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo VR, model 7232 Single Chamber Implantabl...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Marquis DR, model 7274 Dual Chamber Implantable...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync III Marquis, model 7279 Dual Chamber Imp...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync Marquis, model 7277 Dual Chamber Implant...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Marquis VR, model 7230 Single Chamber Implantab...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync II Marquis, model 7289 Dual Chamber Impl...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment