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Mizuho Orthopedic Systems Inc

Mizuho Orthopedic Systems Inc Recalls

All product recalls associated with Mizuho Orthopedic Systems Inc.

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Recall Summary

Total Recalls

1000

Past Year

583

Class I (Serious)

Most Recent

Dec 2025

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 9821–9840 of 10937 recalls

Mizuho Orthopedic Systems Inc: OSI ProFx Operating Room Table 6850 , Pelvic Reconstructi...

Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.

FDAFeb 28, 2007AL, AZ, CA +28 more• Mizuho Orthopedic Systems Inc

Mizuho Orthopedic Systems Inc: OSI, Allegro 6800 Imaging Table (Operating), single pedes...

Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.

FDAFeb 28, 2007AL, AZ, CA +28 more• Mizuho Orthopedic Systems Inc

Mizuho Orthopedic Systems Inc: OSI, 6822 IntraOp Series Tables, Operating Room tables, O...

Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.

FDAFeb 28, 2007AL, AZ, CA +28 more• Mizuho Orthopedic Systems Inc

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Digital Dive Computers (Pelagic) – Decompression Risk (2007)

The recall involves Oceanic-brand ATOM 2.0 dive computers with serial numbers 1 through 2,079 (Revisions 2E, 3A, and 3B) and AERIS-brand EPIC dive computers with serial numbers 1 through 712 (Revision 1A), which can be accessed and viewed on the computer's display. Also, the serial number and date of manufacture are printed on the bottom of the unit (Oceanic ATOM 2.0 from August 23 to November 23, 2006, and AERIS EPIC from October 18 to November 14, 2006). This recall does not include any other Oceanic or AERIS brand dive computers.

CPSCFeb 28, 2007Nationwide• Pelagic Pressure Systems, of San Leandro, Calif.

Philips Medical Systems: Philips HeartStart FR2+ Defibrillator Automated External...

Failure of tactile switches on one of two printed circuit board assemblies (PCBA) used in the FR2+ device. Potential delay or prevention of shock treatment due to PCBA board contamination, causing intermittent switch operation.

FDAFeb 28, 2007Nationwide• Philips Medical Systems

Bio-Logic Systems Corp: Bio-logic-Ceegraph/Sleepscan Netlink Traveler, Bio-logic ...

Battery and Battery Compartment; incorrect placement in the Netlink Traveler unit which caused a short in the wiring of the battery pack and overheating.

FDAFeb 26, 2007Nationwide• Bio-Logic Systems Corp

Gel Candles (M & A Global) – Fire Hazard (2007)

Fire/Burn Risk

This recall involves Everlasting Jelly candles. Models include Champagne Glass with Heart, Model #502; Large Oval Bowl with Sand & Shells, Model #109-XL; Tumbler with Sand & Shells, Model #101-S; Round Shape with Curly Top and Red Roses, Model #506; Round Shape with Penguins, Model #604; Tumbler with Blue Roses & Leaves, Model #805-11; and Round Shape with Two Butterflies, Model #806-8. The candles were sold in clear glass containers of various sizes with a smaller glass of gel in the middle of the candle.

CPSCFeb 22, 2007Nationwide• M & A Global Technologies Inc., doing business as Spa at Home, of Tallahassee, Fla.

American Medical Systems: AMS DURA-II Universal Tips, 2cm, Product Number 72009361,...

Mis-Labeling:The Dura-II 2 cm Universal Tips and the Dura-II 4 cm Distal Tips were incorrectly labeled with the opposite labels.

FDAFeb 19, 2007Nationwide• American Medical Systems

American Medical Systems: AMS DURA-II Distal Tips, 4 cm, Product Number 72009340, S...

Mis-labeling: The Dura-II 2 cm Universal Tips and the Dura-II 4 cm Distal Tips were incorrectly labeled with the opposite labels.

FDAFeb 19, 2007Nationwide• American Medical Systems

General Electric Medical Systems Information Technology: GE Medical Systems Mac-Lab System, cardiac catheterizatio...

GE Healthcare has identified conditions that could cause a potential loss of real-time monitoring with the CardioLab/Mac-Lab/ComboLab Electrophysiology and Hemodynamic Monitoring Systems. These issues are associated with an audio driver, and the use of the application's log and imaging windows.

FDAFeb 16, 2007PR• General Electric Medical Systems Information Technology

General Electric Medical Systems Information Technology: GE Medical Systems CardioLab System, electrophysiological...

FDAFeb 16, 2007PR• General Electric Medical Systems Information Technology

General Electric Medical Systems Information Technology: GE Healthcare Systems ComboLab System. Made up of both M...

FDAFeb 16, 2007PR• General Electric Medical Systems Information Technology

Merit Medical Systems, Inc: StayFix Fixation Device for Percutaneous catheters, REF 6...

Sterility of some units may be compromised due to damaged packaging.

FDAFeb 15, 2007Nationwide• Merit Medical Systems, Inc

Merit Medical Systems, Inc: EpiFix Fixation Device for Epidural Catheters, REF 670M, ...

Sterility of some units may be compromised due to damaged packaging.

FDAFeb 15, 2007Nationwide• Merit Medical Systems, Inc

Becton Dickinson & Company: BD 30ml Syringe Luer-Lok tip Sterile BD, Franklin Lakes, ...

The unit label on a limited number of syringes is incorrect, citing a 20 ml size. All other levels of labeling are correct, identifying the product as 30 ml size.

FDAFeb 15, 2007Nationwide• Becton Dickinson & Company

Stentor Inc A Phillips Medical Systems Co.: The iSight PACS (picture archiving and communications sys...

A defect may cause patient image orientation markers to be incorrectly labeled on Multi-Planar Reformation (MPR) images. Left and Right Anatomical orientation markers may be reversed.

FDAFeb 14, 2007Nationwide• Stentor Inc A Phillips Medical Systems Co.

Orthopedic Systems Inc: Doro Products Adapter, Product number 5979-300. The adap...

Material used to manufacture accessory bracket does not meet product specification. The screw is normally composed of ''Torlon'', which is yellow. The part was made of "Tercite", which is blue.

FDAFeb 14, 2007Nationwide• Orthopedic Systems Inc

Battery Packs for Toy Vehicles (JAKKS Pacific) – fire risk (2007)

Fire/Burn Risk

This recall involves battery packs used with FLY WHEELS XPV toy vehicles. The battery packs were sold with a charger (item number 73904) and with the radio-controlled XPV toy (item number 73906). Item numbers are printed on the product's packaging above the barcode label. The batteries are marked "Fly Wheelz," "XPV," and "JAKKS Pacific," "Lithium-ion Polymer battery (LiPo)" followed by a list of warnings and precautions. The XPV Xtreme Performance Vehicle is not the subject of this exchange program.

CPSCFeb 13, 2007Nationwide• JAKKS Pacific Inc., of Malibu, Calif.

GE OEC Medical Systems, Inc: OEC 9800MD Motorized C-arm System, Fluoroscopic X-ray Sys...

During routine service, a cover may have been installed without the required proper lead shielding.

FDAFeb 9, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC FluoroTrak Plus 9800 Fluoroscopic X-ray System,

During routine service, a cover may have been installed without the required proper lead shielding.

FDAFeb 9, 2007Nationwide• GE OEC Medical Systems, Inc