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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

1000

Class I (Serious)

145

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 36441–36460 of 37661 recalls

Toshiba American Med Sys Inc: Magnetic Resonance Imaging, System: Flexart, Visart and E...

Software anomally causes image slices to be in incorrect order.

FDAJan 27, 2004CA, CO, FL +10 more• Toshiba American Med Sys Inc

Stereotaxis Inc: Cronus Endovascular Guidewire, Length 210 cm (full coat),...

The magnet at the end of the guidewire could break off.

FDAJan 27, 2004Nationwide• Stereotaxis Inc

Stereotaxis Inc: Floppy Cronus Endovascular Guidewire, Length 180 cm (part...

The magnet at the end of the guidewire could break off.

FDAJan 27, 2004Nationwide• Stereotaxis Inc

1...1821 182218231824 1825...1884

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Stereotaxis Inc: Cronus-1 Endovascular Guidewire, Length 210 cm (full coat...

The magnet at the end of the guidewire could break off.

FDAJan 27, 2004Nationwide• Stereotaxis Inc

GE Medical Systems Information Technologies: Dinalink brand Communication Cable which is an accessory ...

The potential exists for external electrical noise to be processed as irregular pacing thereby masking potential asystole events.

FDAJan 27, 2004FL, GA, IN +5 more• GE Medical Systems Information Technologies

Stryker Medical: Stryker brand Adel maternity bed, model 4700, with night ...

A potential shock hazard exists if the night light is damaged.

FDAJan 26, 2004Nationwide• Stryker Medical

Thoratec Corp: Thoratec brand Sealed Arterial Cannula for use with the T...

During use an unexpected flaking of the inner surface coating (blood contact) that has the potential for risk of embolism.

FDAJan 26, 2004Nationwide• Thoratec Corp

Smiths Medical ASD, Inc: Portex Tracheal Tube Guide 15 Fr, non-sterile Catalog Nu...

Tracheal tube guide mislabeled as a 15 Fr instead of a 10 Fr

FDAJan 26, 2004CA, CO, FL +10 more• Smiths Medical ASD, Inc

Stryker Medical: Stryker brand Firstcare Ultra Maternity bed, model 5010, ...

A potential shock hazard exists if the night light is damaged.

FDAJan 26, 2004Nationwide• Stryker Medical

Discovery Kids Pottery Wheel Kit (Curiosity Kits) – Manufacturing Flaw (2004)

Only pottery wheel kits sold during October 2003 with SKU #690974 printed on the white UPC price label attached to the back lower right hand corner of the box are included in this recall. Pottery Wheel Kits sold after October 2003 with different SKU #s are not included in this recall.

CPSCJan 26, 2004Nationwide• Curiosity Kits Inc., of Hunt Valley, Md.

Kyocera Smartphone Batteries – Potential Malfunction (2004)

Fire/Burn Risk

The recalled batteries are included in Kyocera model 7135 Smartphone cell phones. The black and silver flip-up phones say "Kyocera" at the top of the screen. The recalled batteries have the red and white Kyocera name printed on the front and a product code ending with -05 printed on the underside

CPSCJan 23, 2004Nationwide• Coslight International Group, of Hong Kong, manufactured the batteries for Kyocera Wireless Corp., of San Diego, Calif.

Pioneer Surgical Technology: Stayfuse brand intramedullary bone screw; MID 3.8 x 6 mm....

Product labeled as size 3.8x6 mm implant may actually be size 4.3x6 mm implant.

FDAJan 20, 2004Nationwide• Pioneer Surgical Technology

K'NEX Pump Up Racers – Toy Safety (2004)

Laceration Risk

The recalled K'NEX Pump Up Racers come in two models: the "Mud Bogger," which has a yellow car body and the "Street Shredder," which has a red car body. Both models have a date code beginning with 7803, which is located on the bottom of the air motor, directly under the name "K'NEX Industries Inc." The toy cars come with a pump attachment that helps project the car forward.

CPSCJan 20, 2004Nationwide• K'NEX Industries Inc., of Hatfield, Pa.

GVI Technology Partners: CDLCAM, First-Pass Radionuclide Angiography Camera System...

Due to limitations in the operating software, the acquired scan may not be processed properly.

FDAJan 16, 2004Nationwide• GVI Technology Partners

Depuy Orthopaedics, Inc.: P.F.C. Modular Knee System Modular Plus Tibial Wedge 10...

Screw size included in system was incorrect

FDAJan 15, 2004IA• Depuy Orthopaedics, Inc.

Lily Pad Clacker (Kindermusik) – Instrument Risk (2004)

The Lily Pad Clackers are wooden rhythm instruments designed for use with the Frog Went A-Dancing kit sold by Do-Re-Me & You!, a Kindermusik affiliate. The recalled instrument is 5.25 inches long, and is made of wood. It has two green "lily pads" that are connected to the base by a string. The Clackers were sold as part of a music kit.

CPSCJan 14, 2004Nationwide• Kindermusik International, of Browns Summit, N.C.

Bumble Bee Toys (Graco) – Antennae Hazard (2004)

Choking Hazard

All Bumble Bee toys with blue antennae distributed by Graco are included in this recall. Specifically, Bumble Bee toys with blue antennae were distributed with Graco High Chair model numbers 3656CUB, 3658FKB, 3659KER, 3659NGS, 3660WNN and 35605 manufactured between July 22, 2002 and March 9, 2003, and Graco Tot Wheels Mobile Entertainer models 4522OTM, 4522TOTM, 4521ALP, 35628 and 4512FUN manufactured between November 8, 2001 and March 9, 2003. Bumble Bee toys with blue antennae were also distributed separately as an accessory and a replacement part with model number 548094S. Bumble Bee toys with yellow or black antennae are not affected.

CPSCJan 14, 2004Nationwide• Graco Children's Products, Inc. of Exton, Pa.

Perkin Elmer Life and Analytical Sciences Inc: Neonatal Total Galactose Test Kit, contents for 960 assa...

The device is not stable throughout its labeled expiration date.

FDAJan 9, 2004AR, CO, CT +12 more• Perkin Elmer Life and Analytical Sciences Inc

Stryker Howmedica Osteonics: Crossfire Acetabular II Insert. Catalog No: 2041C-2642.

This device is not approved for sale in the US.

FDAJan 9, 2004MI• Stryker Howmedica Osteonics

Kendall Healthcare Products Co: Kendall Curity Disposable Laparotomy Sponges, 12 in x 1...

Sterility compromised due to lack of package seal integrity

FDAJan 8, 2004AL, AZ, CA +23 more• Kendall Healthcare Products Co