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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

1000

Class I (Serious)

127

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 22221–22240 of 25000 recalls

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

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 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.

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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.

Whatman, Inc.: Whatman Body Fluid Collection Paper 903, Ref: 10534790, f...

'903' newborn Neonate screening cards have duplicate numbers assigned on cards and may result in cross-over of patient test results

FDAMay 19, 2009Nationwide• Whatman, Inc.

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

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

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

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.

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.

Computerized Medical Systems Inc: XiO Radiation Treatment Planning System, XiO Release 4.3....

In XiO, when the beams are renumbered, it is possible to get into a state where the dose displayed for a beam does not match the beam placement on the patient. This can occur when dose is calculated, beams are renumbered, and the dose is re-summed only.

FDAMay 13, 2009Nationwide• Computerized Medical Systems Inc

Philips Medical Systems North America Co. Phillips: Accessory Cart for The ACHIEVA 3.0T and Panorama 1T Magne...

The Accessory Cart contained magnetic material and is attracted to the magnet when bringing it close to the system.

FDAMay 12, 2009Nationwide• Philips Medical Systems North America Co. Phillips

Toshiba American Medical Systems Inc: PET-511BTM Multi-plane transesophageal transducer (TEE) u...

Toshiba America Medical Systems Inc is removing the PET-511BTM Multi-plane Transesophageal Transducer from the market after receiving several reports of injury regarding the transducer. Bending or buckling of the flexible portion of the PET-511 BTM multi-plane transesophageal transducer (TEE) may result in injury including perforation.

FDAMay 11, 2009Nationwide• Toshiba American Medical Systems Inc

Acist Medical Systems: ACIST Automated Manifold Kit , REF Model BT2000, SKU # 01...

ACIST Medical Systems initiated a recall due to an increase in the incidence of field reports related to a bulge on the side and/or leaks in the bond of the 2.5 high-pressure tubing of BT2000 kits during a procedure which can result in unsatisfactory performance of the ACIST BT2000 Automated Manifold Kit.

FDAMay 11, 2009AL, AZ, AR +39 more• Acist Medical Systems

Varian Medical Systems Oncology Systems: Varis, Aria Radiation Oncology - Version 8.1.15, 8.5.11, ...

Potential mistreatment-- due to software issues, retired plans may be used and treated repeatedly.

FDAMay 8, 2009Nationwide• Varian Medical Systems Oncology Systems