Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Hitachi Medical Systems America Inc

Hitachi Medical Systems America Inc Recalls

All product recalls associated with Hitachi Medical Systems America Inc.

Get alerts for this brand

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 16241–16260 of 17592 recalls

Hitachi Medical Systems America Inc: MRP-7000 and AIRIS Magnetic Resonance Imaging Systems, So...

Image orientation error. When a 3D Maximum Intensity Projection (MIP) image data set is transferred from the MRI system to a computer workstation via the DICOM protocol, the anatomical markers do not change between the images as they rotate.

FDAAug 16, 2006Nationwide• Hitachi Medical Systems America Inc

Hitachi Medical Systems America Inc: Hitachi Echelon Magnetic Resonance Imaging System, Serial...

Component defect/overheating device; A malfunctioning decoupling circuit in the CTL coil caused high current flow and circuit overheating.

FDAAug 14, 2006Nationwide• Hitachi Medical Systems America Inc

Respironics Novametrix, LLC.: NICO Model 7300 Cardiopulmonary Management System

Audible alarm may not sound during an alert condition

1...811 812813814 815...880

Page 813 of 880Next

FDA

Aug 11, 2006

• Respironics Novametrix, LLC.

Becton Dickinson & Company: BD Vacutainer Push Button Blood Collection Set with Pre-a...

A complaint was received regarding a BD blood collection set where the blister was noticeably warped. The seal width was below minimum specification. Some blisters could adhere together and crack upon separation. Some units may have pre-activated or have defects affecting package integrity.

FDAAug 11, 2006Nationwide• Becton Dickinson & Company

SCC Soft Computer: SoftLab version 4.01 ASCII, ASCII Base 3.1.3.0-3.1.3.32, ...

For SoftLab version 4.01 ASCII, the qualifying test result does not reach the Call List because the order is locked by either another application, or two Hosparams (HISRR_RBS_sync and Auto_sync_RBS). This creates a lock on the RBS server. The problem was identified in the RBS "C" rule which sends qualifying results to the Call List for SoftLab. All affected clients received the upgrade for Soft

FDAAug 4, 2006Nationwide• SCC Soft Computer

Michigan Instruments, Inc.: Michigan Instruments Thumper Mechanical CPR Device; Model...

Failure to initiate compressions when first turned on, if improperly shut down-Operator Manual updated to include proper shut down procedures

FDAAug 4, 2006Nationwide• Michigan Instruments, Inc.

CryoCath Technologies Inc. 16771 Chemin Ste-Marie Kirkland Canada: 7F Freezor Cardiac Cryoablation catheter, REF # 207F1. C...

Outer cartons of catheters were mislabeled with two different reference numbers. The front of the package showed the correct reference number; 207F1, however the section on the top of the box incorrectly referenced 207F3. All inside labels (inside the box and affixed on device pouches) showed the correct reference number, 207F1.

FDAAug 4, 2006Nationwide• CryoCath Technologies Inc. 16771 Chemin Ste-Marie Kirkland Canada

Codman & Shurtleff, Inc.: Codman External Drainage System 3 CSF (EDS 3) With Vent...

Sterility of device is compromised due to package seal defects

FDAAug 4, 2006Nationwide• Codman & Shurtleff, Inc.

Snow Commander Snowthrowers (Toro) – fire hazard (2006)

Fire/Burn Risk

This recall now involves 2001 and 2002 Toro Snow Commander and CCR model snowthrowers listed below. The model and serial numbers are located on the rear of the axle plate between the wheels. SNOW COMMANDER UNITS: Model Serial Range Snowthrower Year Retail Price 38600 220000001 to 220004072 24-inch Single Stage 2002 $860 38602 220000001 to 220005931 24-inch Electric Start 2002 $960 CCR UNITS: Model Serial Range Snowthrower Year Retail Price 38413 210010001 to 210020990 20-inch Single Stage 2001 $590 38419 210010001 to 210014725 20-inch Electric Start 2001 $690 38440 210010001 to 210015656 20-inch Single Stage 2001 $660 38445 210012082 to 210021964 20-inch Electric Start 2001 $760 38515 220000001 to 220013743 20-inch Single Stage 2002 $590 38516 220000001 to 220008930 20-inch Electric Start 2002 $690 38517 220000001 to 220010910 20-inch Single Stage 2002 $660 38518 220000210 to 220015932 20-inch Electric Start 2002 $760

CPSCAug 3, 2006Nationwide• The Toro Company, of Bloomington, Minn.

Robertshaw Gas Controls – fire risk (2006)

Fire/Burn Risk

The FS Flame Switches and FM Automatic Safety Valves being recalled are installed on natural and liquid propane (LP) gas commercial cooking equipment, such as ranges, pasta cookers, deep fat fryers or griddles. The recalled FS Flame Switches were installed on the following commercial cooking equipment brands: Keating (of Chicago), PMI Food Equipment Group, Vulcan, Southbend, Blodgett, Toastmaster, and Wolf Range. The recalled FM Automatic Safety Valves were installed on the following commercial cooking equipment brands: Bari (Restaurant and Pizzeria), Southbend, and Blodgett. The model and/or serial numbers can be found on the cooking appliance identification plate located on the appliance. For a list of appliances with recalled switches and valves, visit www.robertshaw.com

CPSCAug 2, 2006Nationwide• Robertshaw Controls Co., of West Plains, Mo.

Medtronic Sofamor Danek Instrument Manufacturing: Implant Hollow Reamer, 14 mm, REF 8951405, Medtronic Sofa...

Laceration Risk

Bone reamer may not have a cutting surface on the tip.

FDAAug 1, 2006Nationwide• Medtronic Sofamor Danek Instrument Manufacturing

Beckman Coulter Inc: UniCel Dxl 800 Access Immunoassay Systems Wash Buffer, Pa...

The neck of the wash buffer cube can be extended higher than intended possibly causing the system to aspirate air instead of buffer before the buffer container is empty without the system immediately indicating that the supply is empty. This may lead to incorrect assay results.

FDAJul 28, 2006Nationwide• Beckman Coulter Inc

Generac GTH Engines – fuel tank fire risk (2006)

Fire/Burn Risk

The following industrial power equipment products, manufactured by the original equipment manufacturers (OEMs) listed below, are included in this recall: Power Equipment Type OEM/Equipment Seller Pressure Washer Cleaning Systems Specialists, Inc. Phone: (619) 448-8111 Air Compressors Ingersoll-Rand Phone: (800) 820-0308 Pressure Washers Silver Eagle Phone: (936) 264-2215 Saw Mill Wood Mizer Phone: (317) 808-0717 The recalled Generac GTH410 and GTH220 engines were manufactured from July 2001 to July 2005. GTH410 Engines model numbers with defective fuel tanks are: 0041930EHF; 0043290EHF; 0043291; 0045050EHF; 0045281; 0045283; 0046100EHF; 0046150EHF; 0046910EHF; 0046911. GTH220 Engines model numbers with defective fuel tanks are: 0040990EHC; 0043930EHC; 0045300EHC; 0046090EHC; 0046370EHC; 0046380EHC; 0046390EHC; 0046820EHC; 0047640EHC; 0048820; 0050650; 0051170. The engine model number is located on the side of the motor and contained on a small sticker above the Generac nameplate. The top number on the small sticker is the model number (e.g., 220 or 410). The larger Generac nameplate contains the Engine Identification Number and Serial Number.

CPSCJul 27, 2006Nationwide• Generac Power Systems Inc., of Waukesha, Wis.

Beckman Coulter Inc: Cytomics FC 500 Flow Cytometry System with CXP Software V...

Mis-identification-If a panel or protocol is added to an existing worklist but the tube location is not specified, the CXP Acquisition software will run the last specified tube through the remaining protocols and will generate results and printouts of these runs leading to a Mis-Identification condition.

FDAJul 26, 2006Nationwide• Beckman Coulter Inc

John Deere 3000/4000 Tractors (Deere & Co.) – Seat Belt Bracket Failure (2006)

These vehicles are small agricultural tractors that are green with yellow seats and wheels. The following model and serial numbers can be found on the serial number plate on the tractor's frame: Model Serial Numbers 3120 LV3120H210126 through 210552 3320 LV3320E138296 & 245001 through 245250 LV3320F139038 & 250001 through 250015 LV3320H230163 through 231295 LV3320P240043 through 240199 3520 LV3520E270019 through 270240 LV3520F275002 through 275029 LV3520H258079 & 258205 through 258988 LV3520P266001 through 266169 3720 LV3720E290014 through 290325 LV3720H280020 through 280669 4120 LV4120H310005 through 310220 LV4120P317068 through 317435 4320 LV4320E338001 through 338011 LV4320F339002 through 339008 LV4320H320037 through 320562

CPSCJul 25, 2006Nationwide• Deere & Co., of Moline, Ill.

EMD Chemicals Inc: Histochemical PAS (Periodic Acid Schiff) Reaction Set. i...

Due to loose caps, the SO2 levels dropped significantly from release levels causing the product not to perform properly.

FDAJul 25, 2006Nationwide• EMD Chemicals Inc

Becton Dickinson & Company: BD 1mL SafetyGlide Allergy and Tuberculin Syringes. Reor...

BD received reports of needle assembly disengagement from the syringe.

FDAJul 24, 2006Nationwide• Becton Dickinson & Company

Philips Medical Systems: IntelliVue MultiMeasurement Server (MMS)/Multimeasurement...

Patient monitor may display inaccurate reading when the Disposable Sp02 Sensor is not attached

FDAJul 24, 2006Nationwide• Philips Medical Systems

Microvision Medical Holding B.V. Meibergdreef 45 Amsterdam Netherlands: MicroScan Lens Disposable Plastic Cap used with MicroScan...

Some lenses may have microscopic holes in the disposable caps representing a potential break in the sterile barrier

FDAJul 21, 2006CA, IN, IA +4 more• Microvision Medical Holding B.V. Meibergdreef 45 Amsterdam Netherlands

CareFree Warm Mist Humidifier (Hunter) – Fire Hazard (2006)

Fire/Burn Risk

The recalled humidifiers are white or black plastic with blue or green tinted water tanks. "Hunter" and "NiteGlo" are printed on the humidifier. The model numbers and tank size included in this recall are listed below. The model number is located on a white label on the bottom of the humidifier. Model Size Description 35201 CareFree® Humidifier Warm Mist 2.0 Gallon White plastic with a blue tinted water tank 35202 CareFree® Humidifier Warm Mist 2.0 Gallon White plastic with a blue tinted water tank 35203 CareFree® Humidifier Warm Mist 2.0 Gallon White plastic with a green tinted water tank 35207 CareFree® Humidifier Warm Mist 2.0 Gallon White plastic with a blue tinted water tank 35253 CareFree® Humidifier Warm Mist 2.0 Gallon Black plastic with a blue tinted water tank

CPSCJul 18, 2006Nationwide• Hunter Fan Co., of Memphis, Tenn.