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Stryker Communications Corp

Stryker Communications Corp Recalls

All product recalls associated with Stryker Communications Corp.

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Recall Summary

Total Recalls

1000

Past Year

1000

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 17301–17320 of 21320 recalls

Stryker Communications Corp: Amico E-Cylinder Canister Holder, distributed by Stryker ...

Design flaw on the E-Cylinder canister holder may result in early fatigue and failure of the bracket screws, which could cause the cage to become detached from its mount and fall.

FDAMay 19, 2009Nationwide• Stryker Communications Corp

Peak Surgical: PEAK brand PlasmaBlade EXT, Tissue Dissection Device, Cat...

Fire/Burn Risk

A customer reported that a patient suffered a burn while using the device.

FDAMay 19, 2009Nationwide• Peak Surgical

Merit Medical Systems, Inc.: Merit Medical Systems, Inc., Convenience Trays, custom pa...

Surgical gloves in hospital convenience kits may be degraded and tear during use.

FDA

1...864 865866867 868...1066

Page 866 of 1066Next

May 19, 2009

CO, IN, TX

• Merit Medical Systems, Inc.

Medtronic Inc. Cardiac Rhythm Disease Managment: Medtronic KAPPA 600/700/900 Series Implantable Pulse Gene...

One or more bond wire pairs will lift or separate from the bonding terminals on the device hybrid. This may present clinically as loss of rate response, premature battery depletion, loss of telemetry, or no output.

FDAMay 18, 2009GA, WA, PR• Medtronic Inc. Cardiac Rhythm Disease Managment

Medtronic Inc. Cardiac Rhythm Disease Managment: Medtronic SIGMA 100/200/300 Series IPGs, Single Chamber P...

FDAMay 18, 2009GA, WA, PR• Medtronic Inc. Cardiac Rhythm Disease Managment

Siemens Medical Solutions USA, Inc.: ACUSON Sequoia 12.X GI Base System, model number 10042701...

Shock Hazard. The manufacturer failed to set the system power switch to "ON" during the line level leakage and high pot current draw testing.

FDAMay 15, 2009CA, IL, MD +3 more• Siemens Medical Solutions USA, Inc.

Stryker Howmedica Osteonics Corp.: Triathlon Revision Instruments; 1,2,7,8 TGC Upper Tray; N...

Laceration Risk

The screen print for the Valgus Adapter catalog numbers on the Triathlon Trial Cutting Guide Instrument Trays is incorrect.

FDAMay 15, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Siemens Healthcare Diagnostics Inc.: IMMULITE 2000/2500 Chemiluminescent Substrate Module For...

These substrate lots have shown a tendency to introduce a shift in both control and patient results with multiple methods.

FDAMay 15, 2009Nationwide• Siemens Healthcare Diagnostics Inc.

Siemens Medical Solutions USA, Inc.: ACUSON Antares 5.0 Base System, model number 10042832. D...

Shock Hazard. The manufacturer failed to set the system power switch to "ON" during the line level leakage and high pot current draw testing.

FDAMay 15, 2009CA, IL, MD +3 more• Siemens Medical Solutions USA, Inc.

Siemens Medical Solutions USA, Inc.: ACUSON Sequoia 12.X C512/512 SS Base System, model number...

Shock Hazard. The manufacturer failed to set the system power switch to "ON" during the line level leakage and high pot current draw testing.

FDAMay 15, 2009CA, IL, MD +3 more• Siemens Medical Solutions USA, Inc.

Siemens Medical Solutions USA, Inc.: ACUSON Sequoia C512/512SS Adv PE 10.0 System, model numbe...

Shock Hazard. The manufacturer failed to set the system power switch to "ON" during the line level leakage and high pot current draw testing.

FDAMay 15, 2009CA, IL, MD +3 more• Siemens Medical Solutions USA, Inc.

Wright Medical Technology Inc: CONSERVE, TOTAL A-CLASS HEAD W/BFH TECH., REF 38AM-3604, ...

Incorrect packaging, swapped sizes

FDAMay 14, 2009CA, FL, IN +10 more• Wright Medical Technology Inc

Roche Diagnostics Corp.: Roche ACCU-Chek Voicemate Meter, Roche Diagnostics, India...

The lancet cap may be missing, which could result in an unintended lancet stick to the user.

FDAMay 13, 2009Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche ACCU-Chek Aviva Meter Kit, Roche Diagnostics, India...

The lancet cap may be missing, which could result in an unintended lancet stick to the user.

FDAMay 13, 2009Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche ACCU-CHEK Softclix Lancing Device, Distributed by R...

The lancet cap may be missing, which could result in an unintended lancet stick to the user.

FDAMay 13, 2009Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche Coaguchex XS Systems for Patient Self-Testing, Roch...

The lancet cap may be missing, which could result in an unintended lancet stick to the user.

FDAMay 13, 2009Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche ACCU-CHEK Compact Plus Meter Kit, Roche Diagnostics...

The lancet cap may be missing, which could result in an unintended lancet stick to the user.

FDAMay 13, 2009Nationwide• Roche Diagnostics Corp.

Composite Decks (Louisiana-Pacific) – Breaking Risk (2009)

The recall includes outdoor deck board and railings sold under the brand names LP WeatherBest®, ABTCo., and Veranda®. They are composite products that look similar to natural wood and were sold in various colors including Tuscan Walnut/Chestnut, Driftwood Grey/Greystone, Pacific Cedar and Western Redwood. Veranda decking products were manufactured by multiple firms; only products manufactured by LP are included in this recall.

CPSCMay 13, 2009Nationwide• Louisiana-Pacific (LP) Corp., of Nashville, Tenn.

Dixtal Medical, Inc.: Dixtal Novametrix Neonatal/Pediatric SpO2 Sensor, Foam Wr...

Neonatal/Pediatric SPU Sensors may be incorrectly packaged in pouches labeled for Adult/Pediatric SPU Sensors.

FDAMay 13, 2009CT, TX• Dixtal Medical, Inc.

Roche Diagnostics Corp.: Roche ACCU-Chek Active Meter Kit, Roche Diagnostics, Indi...

The lancet cap may be missing, which could result in an unintended lancet stick to the user.

FDAMay 13, 2009Nationwide• Roche Diagnostics Corp.