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Siemens Medical Solutions USA Inc.

Siemens Medical Solutions USA Inc. Recalls

All product recalls associated with Siemens Medical Solutions USA Inc..

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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 17141–17160 of 21320 recalls

Siemens Medical Solutions USA Inc.: Siemens Biograph mCt-X, model number 10248670. Medical I...

In the unlikely event that the device is modified to operate in the tilted position, the telescoping support mechanism will not engage properly.

FDAAug 11, 2009Nationwide• Siemens Medical Solutions USA Inc.

Siemens Medical Solutions USA Inc.: Siemens Biograph mCT-S 64, model number 10248672. Medica...

In the unlikely event that the device is modified to operate in the tilted position, the telescoping support mechanism will not engage properly.

FDAAug 11, 2009Nationwide• Siemens Medical Solutions USA Inc.

Stryker Medical Div. of Stryker Corporation: Stryker Medical wide transport stretcher, Stryker Medical...

The brake/steer pedal may seize, resulting in the brakes not working.

1...856 857858859 860...1066

Page 858 of 1066Next

FDA

Aug 10, 2009

Nationwide

• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical transport stretcher, Stryker Medical, Por...

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Zoom critical care bed, 115v, Stryker Medical, Po...

The backrest of the bed may not stay in an upright position (may drift down when left raised).

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Epic II critical care bed, 115v, Stryker Medical,...

The backrest of the bed may not stay in an upright position (may drift down when left raised).

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical cam bearing service parts, Stryker Medica...

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Ossur H F Grjothals 5 Reykjavik Iceland: Total Knee Junior Model Number 1100 Product Usage: The T...

Some units of the Total Knee Junior produced between November 25th, 2008 and through April, 2009 contain balancing units that may fail under extreme use over a long period. The fault is noncritical and no incidents or injuries resulting from this situation have been reported to Ossur at this stage. Over long term use (estimated to be in the four to six year range) the prosthetic device may fail a

FDAAug 10, 2009Nationwide• Ossur H F Grjothals 5 Reykjavik Iceland

Stryker Medical Div. of Stryker Corporation: Stryker Secure II MedSurg bed, 115 v, Stryker Medical, Po...

The backrest of the bed may not stay in an upright position (may drift down when left raised).

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker MedSurg bed, 115v, Stryker Medical, Portage, MI; ...

The backrest of the bed may not stay in an upright position (may drift down when left raised).

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical M-Series stretcher, Stryker Medical, Port...

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical eye surgery stretcher, Stryker Medical, P...

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical trauma stretcher, Stryker Medical, Portag...

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical , Model 722. Wheeled hospital stretcher.

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Boston Scientific CRM Corp: Guidant LATITUDE Communicator, model 6481, Boston Scienti...

The L ATITUDE communicator (Model 6481) for a patient may not have been able to receive measurements from their weight scale or blood pressure monitor afer initial setup. The issue has been resolved. If any patient weight or blood pressure readings are stored in the patient's sensor, they will be uploaded to LATITUDE after the patient's communicator calls in to Boston Scientific's servers. It

FDAAug 7, 2009Nationwide• Boston Scientific CRM Corp

Airgas Puritan Medical Puritan Medical Unit: AGI-2237 Portable 2 Cylinder Manifold Cart, for connectin...

Yoke may become displaced. Yoke index safety system could become compromised, allowing a user to attach the wrong gas type to the yoke connection.

FDAAug 6, 2009Nationwide• Airgas Puritan Medical Puritan Medical Unit

Airgas Puritan Medical Puritan Medical Unit: AGI-2238 Portable 4 Cylinder Manifold Cart, for connectin...

Yoke may become displaced. Yoke index safety system could become compromised, allowing a user to attach the wrong gas type to the yoke connection.

FDAAug 6, 2009Nationwide• Airgas Puritan Medical Puritan Medical Unit

Medtronic Vascular Galway Limited Parkmore Business Park West Galway Ireland: Endeavor Resolute Zotarolimus-Eluting Coronary Stent Syst...

The product was removed from investigational sites due to a packaging issue, in that the device units were packed without the foil pouch, oxygen absorber and Instructions For Use.

FDAAug 6, 2009Nationwide• Medtronic Vascular Galway Limited Parkmore Business Park West Galway Ireland

Philips Medical Systems (Cleveland) Inc: GEMINI TF Big Bore computer tomograph software version 3....

Two non-safety related defects have been found on the Philips GEMINI TF Big Bore running version 3.6; if these defects were to recur, it could impact the performance or reliability of the system. Philips is issuing a software update to all Philips GEMINI TF Big Bore customers to correct these defects.

FDAAug 5, 2009Nationwide• Philips Medical Systems (Cleveland) Inc

Boston Scientific Corporation: Boston Scientific Impulse Flextrusion Shaft, Angiographic...

Boston Scientific is initiating a recall removal of numerous batches/lots of Wiseguide Guide Catheter, Impulse Angiographic (Diagnostic) Catheter, Expo Angiographic (Diagnostic) Catheter. Boston Scientific has determined that the sterile barrier in the packaging may be compromised. During internal inspections, they discovered gaps between the side seals and the top seal approximately 3/8 in len

FDAAug 5, 2009DC, PR• Boston Scientific Corporation