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Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America Recalls

All product recalls associated with Philips Medical Systems Sales & Service Region No. America.

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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 3461–3480 of 3680 recalls

Philips Medical Systems Sales & Service Region No. America: BV25 Mobile X-Ray System

Potential for c-arm to move due to loose screws

FDAJul 20, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: BV 25 Gold Mobile X-Ray System

Potential for c-arm to move due to loose screws

FDAJul 20, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Biosense Webster, Inc.: Stockert 70 Radio Frequency Ablation Generator

Generator Failure resulting increase of catheter temperature that could not be controlled by power reduction.

FDAJul 16, 2004Nationwide

1...172 173174175 176...184

Page 174 of 184Next

• Biosense Webster, Inc.

GE OEC Medical Systems, Inc: InstaTrak 3500 Navigation and Visualization System

Navigation inaccuracy may result if the headset registration method is used with the Axcess System Kit.

FDAJul 12, 2004CA, CT, KY +7 more• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: InstaTrak 3500 Plus Navigation and Visualization System

Navigation inaccuracy may result if the headset registration method is used with the Axcess System Kit.

FDAJul 12, 2004CA, CT, KY +7 more• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: ENTrak Plus Navigation and Visualization System

Navigation inaccuracy may result if the headset registration method is used with the Axcess System Kit.

FDAJul 12, 2004CA, CT, KY +7 more• GE OEC Medical Systems, Inc

Allen Medical Systems One Post Office Square: Neuro Adapter 2 used with the Berchtold B-810 Surgical Ta...

Neuro adapter may fail to engage and adequately clamp to the surgical table, resulting in movement

FDAJul 12, 2004SC• Allen Medical Systems One Post Office Square

Arch Swing (Playworld Systems) – Structural Weakness (2004)

The 2-3/8" Arch Swing Model # 0289 and the 2-3/8" Arch Swing Add-A-Bay Model # 0380 have arched metal side supports and a welded top rail that supports two swings. The swing sets are made from 2-3/8" steel tubing and come in a variety of solid colors.

CPSCJul 12, 2004Nationwide• Playworld Systems Inc., of Lewisburg, Pa.

GE OEC Medical Systems, Inc: ENTrak Navigation and Visualization System

Navigation inaccuracy may result if the headset registration method is used with the Axcess System Kit.

FDAJul 12, 2004CA, CT, KY +7 more• GE OEC Medical Systems, Inc

Roche Molecular Systems Inc: Amplicor [3] AV-HRP. (Avidin-HRP (Horseradish Peroxidase...

An increased frequency of 'blue foci' that potentially can cause elevated A450 background in microwell plate wells after the addition of conjugate reagent during PCR detection.

FDAJul 7, 2004CT, IN• Roche Molecular Systems Inc

Terumo Cardiovascular Systems Corp: Sarns brand Retrograde Cardioplegia Cannulae, manual -inf...

The product is labeled as sterile, but sterility is compromised because some of the packages were not sealed.

FDAJul 7, 2004Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 9000 Roller Pump; Model 9000; Cat...

Roller Pump: Due to a circuit board malfunction the roller pumps may stop during use without displaying an error message, may stop during use with an overspeed error posted on the local display, or may fail to start/restart resulting in the pump(s) being non-functional.

FDAJul 1, 2004Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 8000 Roller Pump, 115V; Model 800...

FDAJul 1, 2004Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 8000 Roller Pump, 1040V; Model 80...

Due to a circuit board malfunction the roller pumps may stop during use without displaying an error message, may stop during use with an overspeed error posted on the local display, or may fail to start/restart resulting in the pump(s) being non-functional.

FDAJul 1, 2004Nationwide• Terumo Cardiovascular Systems Corp

Varian Medical Systems Inc: medical device and software systems

a malfunction in the software of the VARiS versions 6.2.27 and 6.2.35 which is used to set up radiation therapy devices which will reset parameters to null for future treatments if a patient receives treatment on a non-varian machine and a varian machine and a non-varian field is loaded in the treatment session.

FDAJun 24, 2004Nationwide• Varian Medical Systems Inc

LG TM-510 Cell Phone Batteries (Verizon Wireless) – Battery Malfunction (2004)

Fire/Burn Risk

The recalled batteries can be found in LG TM-510 model cell phones, have a manufacturer/date code of "AEMLLL 02220," AEMMHH 02220," "AEMLLL 02X25H" or "AEMMHH 02725" and were distributed by Verizon Wireless. The manufacturer/date code can be found on the battery, below the words, "Model/Modelo" or "LG." The phone's model number appears on the back side of the phone beneath the battery. The cell phones, which come in black or silver, may have the Verizon Wireless name on the front.

CPSCJun 24, 2004Nationwide• Verizon Wireless of Bedminster, N.J.

Rita Medical Systems: Dispersive Electrodes packaged in an 8x10 plastic container.

Inaccurate temperature readings may be displayed by the device, actual temperature could be 2.5-3 degrees C higher than displayed.

FDAJun 16, 2004Nationwide• Rita Medical Systems

Fobus GLT Gun Holsters (First Samco) – Design Malfunction (2004)

The gun holsters are designed to hold a Series 17 and Series 19 Glock handgun fitted with a laser-sight light. "GL 2*EMZ" is engraved in the top of the gun holster and "FOBUS" and "MADE IN ISRAEL" is printed on the back of the gun holster. This recall involves two early versions of the Fobus GLT gun holsters, one with a plastic retention strap less than one inch wide and one with a leather retention strap less than one inch wide. The new design includes a strap that is more than one inch wide, with a plastic tip too wide to be caught inside the trigger guard.

CPSCJun 9, 2004Nationwide• First Samco, Inc., through its Fobus USA Holster Division, of Southampton, Pa.

Philips Medical Systems Sales & Service Region No. America: ViewForum Review Station Part Numbers: 9896 507 71830, ...

When reviewing images in the module before sending them to PACS or printer the order can be erratic and out of sequence and may cause confusion with the interpretation of the examination.

FDAJun 8, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: MultiDiagnost Eleva Part Numbers: 9896 001 41501 and 98...

When reviewing images in the module before sending them to PACS or printer the order can be erratic and out of sequence and may cause confusion with the interpretation of the examination.

FDAJun 8, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America