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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

620

Class I (Serious)

Most Recent

Dec 2025

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 10681–10700 of 10937 recalls

Philips Medical Systems Sales & Service Region No. America: Philips Digital Diagnost VT

The support chain attachment on the detector carriage may fail and cause the counter weights or detector to fall.

FDANov 20, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Edwards Lifesciences AG Parque Industrial Itabo Km. 18.5 Carr. Sanchez Haina, San Cristobal Dominican Republic: VAMP Direct Draw, Model VMP700 Needleless cannula for sam...

Seal integrity, sterility not assured.

FDANov 20, 2003Nationwide• Edwards Lifesciences AG Parque Industrial Itabo Km. 18.5 Carr. Sanchez Haina, San Cristobal Dominican Republic

Philips Medical Systems Sales & Service Region No. America: Digital Diagnost VE

The support chain attachment on the detector carriage may fail and cause the counter weights or detector to fall.

1...533 534535536 537...547

Page 535 of 547Next

FDA

Nov 20, 2003

Nationwide

• Philips Medical Systems Sales & Service Region No. America

Medtronic MiniMed: Medtronic MiniMed Model 7311Version 5.0A Solutions Pumps ...

Accessory software fails to report certain reports following download of data from 712 pump.

FDANov 19, 2003Nationwide• Medtronic MiniMed

Philips Medical Systems Sales & Service Region No. America: Bucky Diagnost FS Part number 9890-010-83651

Support chain attachment on the Bucky carriage may fail and cause the counter weights or X-ray tube to fall.

FDANov 18, 2003CA, FL, IN +1 more• Philips Medical Systems Sales & Service Region No. America

Bear Jack-In-the-Box (Schylling) – Toy Safety (2003)

Choking Hazard

These multicolor tin Jack-In-the-Box-type toys have illustrations of bears in various activities on the sides. Each side features the enlarged single letters of the word "BEAR" and "BEAR" is written on the top of the toy. Other writing on the sides includes, "Bears in a Boat," "Bears Eating Eggs," "Bears in the Air," and Bears Racing Rabbits." When the crank is turned, the song, "Pop Goes the Weasel" plays, and a toy teddy bear pops up out of the top of the box. "Schylling" is written on the bottom of the toys. Toys with date code stickers on the bottom are not included in the recall.

CPSCNov 18, 2003Nationwide• Schylling Associates Inc., of Rowley, Mass.

Magnum Trail Boss ATP ATVs (Polaris) – Model Year Defect (2003)

Fire/Burn Risk

The recall involves the Polaris model year 2003 and 2004 Magnum 330 4x4 and Magnum 330 Mossy Oak ATVs and model year 2004 Magnum 330 2x4, Trail Boss 330, ATP 330, and ATP 500 ATVs. The recalled ATVs have the following model numbers, which can be found on the certification decal located on the front center body panel: A03CD32(AA)(AC), A04CD32(AA)(AB)(AC), A04CB32(AA)(FC), A04CA32(AA)(AB), A04JD32AA, and A04JD50(AA)(AB)(CA). The name "Polaris" is prominently displayed on the right and left side of the seat and/or on the side body panels.

CPSCNov 12, 2003Nationwide• Polaris Industries Inc., of Minneapolis, Minn.

General Electric Medical Systems Information Technology: Solar 9500 Information Monitor with software version 3A.

Software gives inaccurate readings when transferring TRAM module from Solar 9500 to other Solar monitoring systems without discharging TRAM first.

FDANov 10, 2003Nationwide• General Electric Medical Systems Information Technology

Plan Toys Solid Drums (BRIO) – Design Problem (2003)

Choking Hazard

The recalled Plan Toys Solid Drum is natural wood with blue and red triangles painted on the side. The drum measures 6-1/4 inches in diameter and 3 inches high and has curved holes carved into the top. On the bottom of the drum are three rubber feet attached with screws. The recalled lot numbers are 46271068, 1546214 and 4345141 and are printed on the inside flap of the packaging. A stamp on the bottom of the drum displays the Plan Toys logo.

CPSCNov 6, 2003Nationwide• BRIO® Corp., of Germantown, Wis., a subsidiary of BRIO AB of Sweden

Merit Medical Systems, Inc: UHF Grollman Pigtail Long Tip Non-wirebraid, 7FG, 110 cm,...

Angiographic catheter tips may separate during use.

FDANov 5, 2003FL, MI, NY +4 more• Merit Medical Systems, Inc

Merit Medical Systems, Inc: UHF Cardiac Pigtail non-wirebraid, 7F, 110 cm, Angiograph...

Angiographic catheter tips may separate during use.

FDANov 5, 2003FL, MI, NY +4 more• Merit Medical Systems, Inc

Audio Evacuation Unit (Fire Control) – System Malfunction (2003)

Fire/Burn Risk

All FCI AEUs (part number 1100-1171) manufactured prior to April 12, 2003. These AEUs are used in FireVac 7200 System Control Units. A label in the left center of the circuit board reads "FCI 7200" and "AEU." All V5 versions below V5.2-008 and V6 versions below V6.0.14 are included in the recall.

CPSCOct 30, 2003Nationwide• Fire Control Instruments, of Westwood, Mass.

Russound CAV6.6 Audio Controllers (Russound) – Serial Defect (2003)

The recalled Russound CAV6.6 Controller/Amplifiers have serial numbers ranging between 03141500000000 and 03281500000500, which can be found on the back panel in the upper right hand corner. The black amplifiers also have the words, "CAV6.6 Multizone Controller" printed in silver letters on the front of the unit.

CPSCOct 29, 2003Nationwide• Russound Inc., of Newmarket, N.H.

Wristwatch and Cigarette Lighters (Style Asia) – Design Risk (2003)

Fire/Burn Risk

The Wristwatch lighter is an actual digital wristwatch with a cigarette lighter incorporated into it. The Cigarette-shaped lighter is designed to resemble a filter-tipped cigarette.

CPSCOct 29, 2003Nationwide• Style Asia, Inc. Moonachie, N.J.

Cardiocommand Inc.: The device is labeled as AMS TAPSYSTEM Model 2A Esophagea...

The device may exhibit spurious heart rate increase during esophageal atrial pacing during simultaneous adjacent use of electrosurgical coagulation devices.

FDAOct 27, 2003Nationwide• Cardiocommand Inc.

Teledyne Analytical Instruments: Portable Oxygen Analyzer

Potential failure to display the battery low light to the end-user.

FDAOct 27, 2003AZ, CA, FL +2 more• Teledyne Analytical Instruments

Raptor Utility Vehicles (Koyker) – Off-Road Vehicle Risk (2003)

This recall involves Raptor 1000M off-road utility vehicles. The two-wheel drive vehicles have two seats and a back bed. "Raptor" is printed in black under the vehicles gas cap. Only two wheel drive vehicles with transaxle manufactured between April 12, 2001 and July 31, 2003 are included in this recall.

CPSCOct 21, 2003Nationwide• Koyker Manufacturing Company, of Lennox, S.D.

Datex-Ohmeda Inc One Ohmeda: Datex-Ohmeda Cardiocap/5 Patient Monitors

Datex-Ohmeda Cardiocap/5 Patient Monitors have bracket pins which do not adequately secure them to their optional mounting stand so the monitors may fall.

FDAOct 17, 2003Nationwide• Datex-Ohmeda Inc One Ohmeda

Ohmeda Medical, A Div of Datex-Ohmeda Inc: Radiant Heater Door Vent for Ohmeda Medical''s Giraffe (t...

Heater vent door on neonatal incubator may malfunction.

FDAOct 17, 2003Nationwide• Ohmeda Medical, A Div of Datex-Ohmeda Inc

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1 Roller Pump; 4 inch di...

The roller pump tube clamp mechanism may fail to release , making it difficult to remove or insert the tubing, and thereby delaying perfusion.

FDAOct 16, 2003Nationwide• Terumo Cardiovascular Systems Corp