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Stryker Howmedica Osteonics

Stryker Howmedica Osteonics Recalls

All product recalls associated with Stryker Howmedica Osteonics.

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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 3521–3540 of 3680 recalls

Stryker Howmedica Osteonics: Restoration Hip system Cylindrical Distal Extension. Cat...

The Cylindrical Distal Extensions were incorrectly coded and packaged.

FDAFeb 10, 2004Nationwide• Stryker Howmedica Osteonics

General Electric Med Systems: Seneographe 500 Mammography X-Ray Systems (all versions)

The mammography system's information for users lacked the technical specification for the minimum filtration permanently installed in the useful beam and the technical specification for the maximum line current.

FDAFeb 6, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Seneographe DMR Mammography X-Ray System (all versions)

1...175 176177178 179...184

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FDAFeb 6, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Seneographe 2000D Digital Mammography X-Ray System

FDAFeb 6, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Seneographe 800T Mammography X-Ray Systems

FDAFeb 6, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Seneographe 600 Mammography X-Ray Systems (all versions)

FDAFeb 6, 2004Nationwide• General Electric Med Systems

Varian Medical Systems: EPROM and Control Software (embedded), version 5.08, for ...

Radiation treatment software could potentially cause a healthcare practitioner to apply incorrect treatment regimen to patients undergoing brachytherapy.

FDAFeb 6, 2004Nationwide• Varian Medical Systems

General Electric Med Systems: Seneographe 700T Mammography X-Ray Systems

FDAFeb 6, 2004Nationwide• General Electric Med Systems

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

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 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

DWL Systems, Inc.: EZ-DOP, diagnostic ultrasound imaging system

A certain sequence of data entries on the keypad could cause the ultrasound medical device to display incorrect transmission power.

FDAJan 5, 2004Nationwide• DWL Systems, Inc.

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1 Electronic Oxygen Blen...

The flow meter could malfunction resulting in loss of touchscreen control of the gas system, but the alternate mechanical control will remain operable.

FDAJan 1, 2004Nationwide• Terumo Cardiovascular Systems Corp

Stryker Howmedica Osteonics: Restoration T3 Revision Hip System, Femoral Hip Prosthesi...

Restoration T3 Revision Hip System distal stem has demonstrated fractures.

FDADec 30, 2003Nationwide• Stryker Howmedica Osteonics

Access CardioSystems: Access AED and Access ALS Automated External Defibrillato...

Difibrillator may fail to operate due to a faulty component on the circuit board

FDADec 19, 2003AL, CA, FL +4 more• Access CardioSystems

Advanced Sterilization Products: Cidex Plus Test Strips

May not accurately detect minimum effective concentration (MEC)

FDADec 17, 2003Nationwide• Advanced Sterilization Products

General Electric Med Systems: Performix X-ray Tube - Performix ADV, Performix Ultra, So...

Incorrect mounting hardware may cause X-ray tube to separate from the gantry and fall.

FDADec 8, 2003Nationwide• General Electric Med Systems

Danatech Medical Systems Inc: Product is a handheld fetal Doppler used to screen for fe...

This prescription device, without an approved 510K , was distributed to unauthorized consumers, mostly pregnant women, on the internet.

FDADec 5, 2003Nationwide• Danatech Medical Systems Inc