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Hitachi Medical Systems America Inc

Hitachi Medical Systems America Inc Recalls

All product recalls associated with Hitachi Medical Systems America Inc.

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Recall Summary

Total Recalls

1000

Past Year

353

Class I (Serious)

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 3221–3240 of 3680 recalls

Hitachi Medical Systems America Inc: Hitachi CXR-4 CT Computed Tomography X-ray System (includ...

The device has a software anomaly which affects the system's ability to create Multiplanar Reconstructions (MPR). Some images from the resulting series do not display correctly, or display at all, when MPR was run on them.

FDAFeb 21, 2006Nationwide• Hitachi Medical Systems America Inc

Stryker Howmedica Osteonics Corp.: Scorpio X3 UHMPWE Tibial Inserts and Scorpio X3 UHMWPE Pa...

Stryker Orthopaedics became aware of a potential anomaly related to the packaging process of referenced lots of X# polyethylene used on Scorpio, Triathlon and Trident inserts.

FDAFeb 17, 2006Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Triathlon X3 UHMWPE Tibial Inserts and Patellar Component...

Stryker Orthopaedics became aware of a potential anomaly related to the packaging process of referenced lots of X# polyethylene used on Scorpio, Triathlon and Trident inserts.

1...160 161162163 164...184

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FDAFeb 17, 2006Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Trident Acetabular Hip System Polyethylene Inserts, Stryk...

Stryker Orthopaedics became aware of a potential anomaly related to the packaging process of referenced lots of X# polyethylene used on Scorpio, Triathlon and Trident inserts.

FDAFeb 17, 2006Nationwide• Stryker Howmedica Osteonics Corp.

Orchestro Espresso Makers (Eugster/Frismag) – Fire Hazard (2006)

Fire/Burn Risk

The recalled espresso makers are black and silver, have a silver control panel, and can make two cups of espresso at once. The word "KRUPS" is printed on the front of the machine. The model number and factory mark are stamped on a silver sticker on the bottom of the machine. The following are the recalled models: Model Number Factory Mark 889-45 F8894556 890-41 F8904156

CPSCFeb 15, 2006Nationwide• Eugster/Frismag of Switzerland

Lasko Floor Fans (Lasko) – Fire Risk (2006)

Fire/Burn Risk

This recall involves various models of Lasko, Galaxy, Air King and General Electric fans manufactured between January 1999 and July 2001, and sold through February 2004. Styles and model numbers of recalled fans, which are either stamped or on a label on the bottom of the fans, are listed below: Brand Type of Fan Model Numbers Lasko Box Fan Cyclone Fan Wind Machine Air Companion Air Director Wind Tunnel Models 3700, 3723, 3733, 3750 Models 3510, 3550, 3800, 35105 Models 3300 and 3521 Model 3515 Model 2135 Models 3400 and 3410 General Electric Box Fan Cyclone Fan Model 106620 Models 106600, 106630 Galaxy Box Fan Model 3733 Air King Cyclone Fan (20" deluxe pivot fan) Air Companion (15" deluxe pivot fan) Model 9500 Model 9515 Detailed information and pictures of affected models can be found at www.laskoproducts.com

CPSCFeb 8, 2006Nationwide• Lasko Products Inc., of West Chester, Pa.

GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226: Datex-Ohmeda S/5 Critical Care Monitor with L-CICU01, L...

GE Healthcare (Datex-Ohmeda) S/5 Critical Care Monitor and S/5 Compact Critical Care Monitor with L-CICU01, L-CICU02A, L-ICU05 & L-ICUO5A software had an issue where the Heart Rate (HR) was displaying as ---(3 dashes) when the monitor was used continuously for 49 days without a cold start. A missed alarm or missed HR value could cause a delay in recognition of a cardiac event that may result i

FDAFeb 6, 2006IA, PR• GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226

GE OEC Medical Systems, Inc: GE Healthcare Navigation Pin Transmitter (GE P/N 1004070)...

Small retaining pin may detach and fall into the surgical field during stereotactic surgery.

FDAFeb 6, 2006AL, AZ, CA +23 more• GE OEC Medical Systems, Inc

Philips Medical Systems North America Co. Phillips: Allura Xper FD10/10 x-ray system

Potential lock-up of system requiring reboot of system.

FDAFeb 6, 2006Nationwide• Philips Medical Systems North America Co. Phillips

GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226: Datex-Ohmeda S/5 Compact Critical Care Monitor with L-CIC...

FDAFeb 6, 2006IA, PR• GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226

Philips Medical Systems North America Co. Phillips: Allura Xper FD10 x-ray system

Potential lock-up of system requiring reboot of system.

FDAFeb 6, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Fujifilm Medical System USA, Inc.: Synapse Software Versions 3.1.0 and 3.1.1 used with the F...

Image orientation and orientation markers may not match when an image is rotated or flipped when the CT Image is preset.

FDAFeb 3, 2006Nationwide• Fujifilm Medical System USA, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK 500 automated external defibrillator (AED)

Component leads may have intermittent connection to the printed circuit board assembly pads - which could render the device inoperative.

FDAFeb 1, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK CR Plus defibrillator

One of the printed circuit board assemblies may be contaminated with solder flux which can cause a short that may render the device inoperative.

FDAJan 31, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK EXPRESS defibrillator

One of the printed circuit board assemblies may be contaminated with solder flux which can cause a short that may render the device inoperative.

FDAJan 31, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Hitachi Medical Systems America Inc: Hitachi Altaire Magnetic Resonance Imaging System

Circuit Failure-There is the potential risk of the Phase Loss Detector Safety Device (PHSEN PCB) malfunctioning in the event of a power loss. The circuit may fail to turn off the system main breaker when 2 of the 3 power phases are lost.

FDAJan 27, 2006Nationwide• Hitachi Medical Systems America Inc

General Electric Med Systems LLC: Discovery ST PET/CT imaging system with gantry model numb...

The LightSpeed CT Technical Reference Manual was omitted from the document kit shipped with the PET/CT system.

FDAJan 26, 2006Nationwide• General Electric Med Systems LLC

American Medical Systems: her option Cryoablation Therapy Disposable Probe, Model C...

Fire/Burn Risk

Overheating of the Cryoablation Therapy Disposable Probe (CU-1), could cause a burn injury to a patient or user in certain circumstances.

FDAJan 13, 2006Nationwide• American Medical Systems

Direct Connect 8 Power Strips – Shock Hazard (2006)

The Direct Connect 8 (DC8) power strip is sold for use to control aquarium equipment with a computer. The power strip has a black aluminum enclosure with eight outlets, and a black extension cord. The serial number is printed on the white label on the side of the unit. The serial numbers are between DC81000 through DC81633. "Direct Connect 8" is written on the side of the unit.

CPSCJan 11, 2006Nationwide• Neptune Systems, of San Jose, Calif.

Guardian Generator Fuel Hoses – Safety Concern (2006)

Fire/Burn Risk

The recalled 12-inch braided flex fuel hoses are used with Guardian® Home Standby Air-Cooled Generators with serial numbers 3789827 and below. The generators are about 4 feet by 2 feet by 2½ feet, tan in color, and have identification decal tags displaying the serial number. The decal tag is affixed to the black divider plate that separates the engine from the control panel and can be found by lifting the top/lid of the metal enclosure. The fuel hose came supplied with the generator kits and connects the fuel supply to the generator. The hose is 12 inches long and covered with braided steel.

CPSCJan 11, 2006Nationwide• Generac Power Systems Inc., of Waukesha, Wis. (generator)