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Toshiba American Med Sys Inc

Toshiba American Med Sys Inc Recalls

All product recalls associated with Toshiba American Med Sys Inc.

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Recall Summary

Total Recalls

1000

Past Year

899

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 17041–17060 of 17592 recalls

Toshiba American Med Sys Inc: Magnetic Resonance Imaging System Core Software, Sof...

Software anomaly.

FDAMay 6, 2004Nationwide• Toshiba American Med Sys Inc

Beckman Coulter Inc: Customized Automation Centrifuge, First and Second Genera...

Centrifuge loss of containment with potential for injury or exposure to biohazard among lab workers.

FDAMay 6, 2004Nationwide• Beckman Coulter Inc

Fujifilm Medical System USA, Inc.: Fuji Flash IIP and CR-IR346CL Consoles

Software: Incorrect measurement of objects within a CR image

FDAMay 5, 2004Nationwide• Fujifilm Medical System USA, Inc.

1...851 852853854 855...880

Page 853 of 880Next

Varian Medical Systems: VariSource High Dose Rate Afterloader, Models 200, 200t, ...

Manufacturer of brachytherapy instrument issued a Customer Technical Bulletin to clarify instructions for use of the radiation treatment medical device by healthcare practitioners.

FDAMay 4, 2004Nationwide• Varian Medical Systems

Cypress Medical Products, Ltd.: Manual Mechanical Wheelchair, 24'' seat, , maximum patien...

The seat of the wheelchair may come loose from the frame with the screws and the collars still attached when the seat is pulled upward to fold the wheelchair.

FDAMay 3, 2004Nationwide• Cypress Medical Products, Ltd.

Cypress Medical Products, Ltd.: Manual Mechanical Wheelchair, 18'' seat, , maximum patien...

The seat of the wheelchair may come loose from the frame with the screws and the collars still attached when the seat is pulled upward to fold the wheelchair.

FDAMay 3, 2004Nationwide• Cypress Medical Products, Ltd.

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1; 100V -120V, 15 A (cir...

The battery status light on the front panel may not accurately reflect the actual status of the battery. The battery may contain more charge than indicated.

FDAMay 1, 2004Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1; 100V -120V, 15 A (cir...

The gas system may fail calibration prior to use due to incorrect gas system flowmeter software.

FDAMay 1, 2004Nationwide• Terumo Cardiovascular Systems Corp

ACMI CORPORATION: ACMI REF E-9F Electrohydraulic Lithotripsy Probe, 9 FR...

Product sterility may be compromised due to the lack of package seal integrity

FDAApr 30, 2004Nationwide• ACMI CORPORATION

ACMI CORPORATION: ACMI REF E-3F Electrohydraulic Lithotripsy Probe, 3 FR ...

Product sterility may be compromised due to the lack of package seal integrity

FDAApr 30, 2004Nationwide• ACMI CORPORATION

ACMI CORPORATION: ACMI REF E-5F Electrohydraulic Lithotripsy Probe, 5FR x...

Product sterility may be compromised due to the lack of package seal integrity

FDAApr 30, 2004Nationwide• ACMI CORPORATION

ACMI CORPORATION: ACMI REF E-1F Electrohydraulic Lithotripsy Probe, 1.9 F...

Product sterility may be compromised due to the lack of package seal integrity

FDAApr 30, 2004Nationwide• ACMI CORPORATION

American Medical Systems: AMS Ambicor Penile Prosthesis, Penoscrotal Approach, Leng...

The product is mislabeled as to length.

FDAApr 29, 2004CA, IN, TX +1 more• American Medical Systems

Fireplace Remote Receivers (CFM) – Safety Defect (2004)

Fire/Burn Risk

Majestic Vermont Castings fireplace remote receivers were sold with the HES40R and HES40 electric fireplaces/stoves and sold as accessory items for CFM DEF33/36, DEF36S2, Addision, DEF26, and HE32EF electric fireplaces and stoves. The recalled remote receivers have the words "Majestic Vermont Castings" on a label affixed to the face of the receiver. Model number ERX15 B can be found on the CSA approval sticker on the back of the remote receiver.

CPSCApr 28, 2004Nationwide• CFM Corporation, of Mississauga, Ontario, Canada

Gas Water Heater Controls (White-Rodgers) – Temperature Risk (2004)

Fire/Burn Risk

The temperature control is a small metal box located above the access panel door of the gas water heater. A white label with red lettering located on the right side of the control contains one of the following model numbers: 37C55U 658, 37C57U 602, 37C72U 520, 37C72U 546, 37C72U 547, or 37C72U 548, and 37C72U 676. There should be a four- digit metal stamped date code located below the label on the right side of the control. Recalled controls will have date codes 0240 to 0329 (40th week of 2002 to 29th week of 2003). Potentially affected gas water heaters include: AO Smith, Apollo, Crosley, Energysense, Freedom, Intertherm, Kenmore, Maytag, Mission, Myers, Penfield, President, Reliance, Sentry, or State. Beginning serial numbers on these gas water heaters can be checked at www.regcen.com/tempcontrolrecall

CPSCApr 28, 2004Nationwide• White-Rodgers, a division of Emerson Electric Co., of St. Louis, Mo.

MRL, Inc., A Welch Allyn Company: Welch Allyn AED 10 Defibrillator; a battery powered autom...

A faulty component has been identified which could result in an intermittent shock button (button #3) failure on the AED10 defibrillator.

FDAApr 26, 2004Nationwide• MRL, Inc., A Welch Allyn Company

Fischer Imaging Corporation: VersaRad/Traumex General Radiographic System.

If two of the four T-nuts that connect the transverse rail to the ceiling rail fail, the 'U' arm and transverse rails could fall and cause serious injury.

FDAApr 23, 2004Nationwide• Fischer Imaging Corporation

Wilson-Cook Medical Inc: Biliary Stent Introducer Set

The guiding catheter provided with the SIS-10 biliary stent introduction system may be a 5 French instead of the required 6 French guiding catheter.

FDAApr 21, 2004MO, NY, PA• Wilson-Cook Medical Inc

Wilson-Cook Medical Inc: AcuSnare Polypectomy Device, Cook Wilson-Cook Medical GI ...

The snares inside the box labeled SASM-1 may actually be ASM-1 devices. The individual pouches may be correctly labeled ASM.

FDAApr 21, 2004MA, NY, OK• Wilson-Cook Medical Inc

Beckman Coulter Inc: Coulter AcT 5diff Autoloader (AL) Hematology Analyzer

Software anomaly causes sample results to be not credible, reported as '0' or left blank. The next sample will also be incorrectly reported for the same parameter.

FDAApr 20, 2004Nationwide• Beckman Coulter Inc