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Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips Recalls

All product recalls associated with Philips Medical Systems North America Co. Phillips.

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Recall Summary

Total Recalls

1000

Past Year

893

Class I (Serious)

124

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 15001–15020 of 17593 recalls

Philips Medical Systems North America Co. Phillips: ALLURA XPER FD20/10 The intended uses of the Allura XPER ...

The Printed Circuit Board (PCB) in the Main-cabinet. Further investigation revealed that a manufacturing error in the PCB is responsible for the reliability issue. As a result, the complete system may shut down and not re-start.

FDAMay 26, 2009Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: ALLURA XPER FD10/10 The intended uses of the Allura XPER ...

FDAMay 26, 2009Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura XPER FD10 F/C The intended uses of the Allura XPER...

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FDAMay 26, 2009Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: MultiDiagnost Eleva with FD. The Philips MultiDiagnost E...

FDAMay 26, 2009Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura XPER X-ray system. The intended uses of the Allura...

FDAMay 26, 2009Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: ALLURA XPER FD20 The intended uses of the Allura XPER X-r...

FDAMay 26, 2009Nationwide• Philips Medical Systems North America Co. Phillips

Toshiba American Medical Systems Inc: Toshiba America Medical Systems Inc (TAMS) Digital Radiog...

Toshiba America Medical Systems Inc (TAMS) has initiated a field correction on the DRAD-3000E; Radrex-I, Electrostatic x-ray imaging system due to a software bug that results in a loss of image.

FDAMay 22, 2009Nationwide• Toshiba American Medical Systems Inc

Jitterbug Phones (Samsung) – 911 service issue (2009)

This recall involves "Jitterbug" cell phones model numbers SPH-a110 and SPH-a120 with standard key pads and version BB14 software. No other Samsung wireless phones or software versions are included in this recall.

CPSCMay 22, 2009Nationwide• Samsung Telecommunications America, of Richardson, Texas

Blackstone Medical, Inc.: Blackstone Medical: ICON Modular Pedicle Screw System; P...

Product marketed without an approved 510(k)

FDAMay 21, 2009Nationwide• Blackstone Medical, Inc.

Bunk Beds (Gothic Cabinet Craft) – Fall Risk (2009)

Both metal and wooden bunk beds are being recalled. The bunk bed styles include dark oak and metal, solid pine, others come with six drawers as part of the base.

CPSCMay 21, 2009Nationwide• Gothic Cabinet Craft Inc., of Maspeth, N. Y.

Acumed LLC: Polarus(R) Humeral Fixation System, size: 3.5mm x 25.0mm ...

Laceration Risk

Mix-up of parts - Product labeled cortical bone screw actually contains Acutract fixation screw

FDAMay 19, 2009FL, GA, MI +4 more• Acumed LLC

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

Bicycle Frames (Norco) – Crash Hazard (2009)

The recalled bicycle frames include the following model year and model names: 2007 Team DH, 2008 Team DH, Aline Park, Aline, Atomik, Shore 1,2,3, 2009 Atomik (without gussets). All colors are included in the recall and the model name is printed on a decal on the top tube of each frame/bike.

CPSCMay 19, 2009Nationwide• Norco Performance Bikes, of British Columbia, Canada

Bicycles (Cannondale) – Crash Risk with JD Forks (2009)

The recall involves model year 2008 Cannondale Adventure 2, Adventure 3, Adventure 2 Feminine and Adventure 3 Feminine bicycles. The model name is printed on the bicycle's frame. The bicycles have a suspension fork with the words "cannondale AT35 adventure trail" printed on them. Bicycles equipped with the Rock Shox i-ride fork are not included in the recall.

CPSCMay 19, 2009Nationwide• JD Components, of Taiwan

Bicycles (Trek) – Crash Risk with JD Forks (2009)

The recall involves model year 2009 Trek 7300, 7300WSD, and 7500 bicycles. The model name is printed on the bicycle's frame. The bicycles have a suspension fork with the words "Bontrager SPA" printed on them.

CPSCMay 19, 2009Nationwide• JD Components, of Taiwan

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.

FDAMay 19, 2009CO, 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

Carl Zeiss Meditec Inc: VISU 200 on S8 Floor Stand, Manufactured by Carl Zeiss Su...

Potential Retina Damage-- An error in the user manual may result in misapplied filter and injury during treatment.

FDAMay 18, 2009Nationwide• Carl Zeiss Meditec Inc

Widetrak Snowmobiles (Polaris) – Shock Hazard (2009)

This recall involves model year 2009 Polaris IQ WIDETRAK snowmobiles with the engine block or battery heater directly installed. Model number S09PU7ES is printed on the right side of the tunnel below the seat. This recall also involves Polaris accessory engine block heaters and battery heaters.

CPSCMay 13, 2009Nationwide• Polaris Industries Inc., of Medina, Minn.