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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

309

Past Year

Class I (Serious)

Most Recent

Oct 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 241–260 of 309 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

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

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

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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

Integrated Measurement Systems, Inc.: IMS Patient Scale used on Sunrise Medical's Hoyer Presen...

Patient Scale may become detached, which can cause a patient to fall and result in injury.

FDAJan 30, 2007Nationwide• Integrated Measurement Systems, Inc.

Advanced Neuromodulation Systems, Inc: Eon Rechargeable Implantable Pulse Generator (IPG) System

Product's external charging system on occasion was failing to communicate with the Implantable Pulse Generator preventing re-charging of the pain relief system.

FDADec 22, 2006Nationwide• Advanced Neuromodulation Systems, Inc

Computerized Medical Systems Inc: AccuSeed DS Digital Stepper, an accessory to a prostate r...

The In/Out adjustment knob can be over-turned, ultimately causing the incorrect placement of radioactive seeds in the patient.

FDANov 9, 2006Nationwide• Computerized Medical Systems Inc

Varian Medical Systems Inc: 4D Integrated Treatment Console and Varis 1.4g Medical Ch...

Selecting an empty space next to the ''Override'' or ''Acquire Actual'' buttons may result in mistreatment to the patient.

FDASep 21, 2006Nationwide• Varian Medical Systems Inc

Varian Medical Systems Inc: Clinac High Energy Medical Linear Accelerator, Medical Ch...

The chain holding the device gantry in position may break.

FDAAug 31, 2006Nationwide• Varian Medical Systems Inc

Disetronic Medical Systems, Inc.: Disetronic D-TRONplus Insulin Pump Battery Pack; Ref/Cata...

The battery may turn the pump off without warning due to a design change in the battery.

FDAJul 13, 2006Nationwide• Disetronic Medical Systems, Inc.

Varian Medical Systems Inc: Varian brand Clinac C-series Pendant Radiation delivery s...

Machine may produce unexpected motions from the couch, collimator, and gantry rotation at maximum speeds.

FDAJun 6, 2006Nationwide• Varian Medical Systems Inc

Rita Medical Systems, Inc.: Talon Straight, 25 cm--Electrosurgical Device--RITA * Med...

Misbranding; Product may have the wrong device handle which incorrectly identifies the product and also has incorrect deployment depth marker.

FDAMay 2, 2006AL, AR, FL +8 more• Rita Medical Systems, Inc.

Rita Medical Systems, Inc.: XLie with Tubing, 12 cm, Electrosurgical Device-RITA * Me...

Misbranding; Product may have the wrong device handle which incorrectly identifies the product and also has incorrect deployment depth marker

FDAMay 2, 2006AL, AR, FL +8 more• Rita Medical Systems, Inc.

Emergency Smoke Hoods (EVAC) – Carbon Monoxide Risk (2006)

Fire/Burn Risk

These smoke hoods are one-time use respiratory devices that assist users with breathing, while escaping a fire. They include a transparent plastic hood that covers the user's head, and a canister that filters out toxic gases. "EVAC+™" or "EVAC-U8™" is printed on the canister.

CPSCApr 20, 2006Nationwide• Brookdale International Systems Inc., of Vancouver, British Columbia, Canada

Bard Access Systems, Inc: 24F Tri-Funnel Replacement Gastrostomy Tube

Packaging for some gastrostomy tubes was labeled with incorrect balloon inflation data. An underinflated balloon may cause misplacement, slippage or premature removal of the tube. If an underinflated balloon allows the tube to be placed, or slip into, the stomal tract and not the stomach, there is a risk of infusion of fluids into the peritoneum. This carries the risk of infection.

FDAApr 6, 2006Nationwide• Bard Access Systems, Inc

Disetronic Medical Systems, Inc.: Disetronic Ultraflex 8/110 infusion set; (Distributed ou...

The luer tube may break at the lock-tubing connection to the pump, causing an interruption of insulin delivery, which can and has contributed to hyperglycemia

FDAMar 31, 2006Nationwide• Disetronic Medical Systems, Inc.

Disetronic Medical Systems, Inc.: Accu-Chek Ultraflex soft DUS 1 infusion set; 8 mm (60 cm)...