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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

899

Class I (Serious)

125

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 17261–17280 of 17592 recalls

Philips Medical Systems Sales & Service Region No. America: Diagnost 97

Labeling of push button caps located on the control panel may not clearly identify the applied Source to Image distance (SID).

FDAJul 17, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: OmniDiagnost System

Labeling of push button caps located on the control panel may not clearly identify the applied Source to Image distance (SID).

FDAJul 17, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Toad Lawn Ball Sprinkler (Midwest) – Design Defect (2003)

The green, frog-shaped sprinkler is 6-1/2 inches long, 6-1/2 inches wide and 7 inches tall. The recalled lawn balls have a label on the bottom that includes the model number 738449 508893 and the words, "Made in China."

1...862 863864865 866...880

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CPSC

Jul 17, 2003

Nationwide

• Midwest, of Cannon Falls, Minn.

TimeCutter Z Riding Mower (Toro) – Model Range Issue (2003)

Laceration Risk

Model Serial Range Description 74301 230000001-230003210 14 HP 38-inch cut zero-turn radius tractor 74325 230000001-230000500 16 HP 42-inch cut zero-turn radius tractor 74330 230000001-230003070 16 HP 42-inch cut zero-turn radius tractor 74350 230000001-230001145 17 HP 42-inch cut zero-turn radius tractor The model and serial number decal can be found on the frame below the seat.

CPSCJul 15, 2003Nationwide• Toro Company, of Bloomington, Minn.

Datex-Ohmeda Inc One Ohmeda: Datex-Ohmeda S/5 Anesthesia Delivery Units

Possible disruption of mechanical ventilation or disruption of anesthetic agent delivery.

FDAJul 15, 2003Nationwide• Datex-Ohmeda Inc One Ohmeda

Diametrics Medical, Inc.: IRMA SL Blood Analysis System CC pH, pCO2, pO2, Hct, Na+,...

An incorrect lot designation, when entered into the blood analysis device, caused the device to give an error message and not operate.

FDAJul 14, 2003CA, CO, FL +6 more• Diametrics Medical, Inc.

Blue Torch Medical Technologies: CaverMap Surgical Aid Disposable Kit with Focused Probe T...

Product's sterility is compromised due to a failed sterility audit

FDAJul 10, 2003NY, TX• Blue Torch Medical Technologies

Sleep Number Beds (Select Comfort) – Cold Weather Problem (2003)

Laceration Risk

This program includes all Sleep Number® Beds by Select Comfort sold from November 2002 through March 15, 2003 that were shipped through or to cold weather locations.

CPSCJul 9, 2003Nationwide• Select Comfort Corporation, of Minneapolis, Minn.

Misys Healthcare Systems: Misys Laboratory System, Versions 5.2, 5.23, 5.3 up to 5....

Software defect causes orders to be lost under certain conditions of use. A typographical error at the Accept/Modfy/Reject prompt will cause the order not to be processed by the system.

FDAJul 7, 2003Nationwide• Misys Healthcare Systems

Rear Projection TVs (Toshiba) – Model Safety Concern (2003)

Laceration Risk

This program includes a limited number of units of the following Toshiba rear projection televisions: Model 50A62, Model 51H83, and Model 57H83. To determine if your television set is affected by this corrective action, go to www.tacp.toshiba.com/safety_notice.asp and follow the instructions.

CPSCJul 3, 2003Nationwide• Toshiba America Consumer Products, Inc., of Wayne, N.J.

Misys Healthcare Systems: Misys Laboratory System version 5.3

Patient files become mixed up due to a software defect.

FDAJul 2, 2003NY• Misys Healthcare Systems

International Adapter Plugs (Franzus) – Electrical Safety Issue (2003)

Laceration Risk

The black or white plastic adapter plugs have names of specific countries or regions where the plugs are intended for use written on the side. The writing includes "NORTHERN EUROPE," "GREAT BRITAIN," "NO. AMERICA," "AUSTRALIA," and "SO. EUROPE." Except for the names of these countries and regions, the recalled plugs have no other writing on them. Plugs with "MADE IN USA" printed between the prongs, or that have a screw between the prongs, are not included in the recall.

CPSCJul 2, 2003Nationwide• Franzus Company LLC, of Beacon Falls, Conn.

Spit Smatter Spray Foam (JAKKS Pacific) – Pressurized Foam Risk (2003)

The "Spit Smatter" spray comes in a pressurized can and emits a colored foam based on one of five brands: "Original Smatter," "Blueberry Smatter," "Banana Cream Smatter," "Lemon Meringue Smatter," and "Fatter Smatter." The brand name is printed on the can and the word "Nickelodeon" is printed on the orange trigger mechanism.

CPSCJul 2, 2003Nationwide• JAKKS Pacific Inc., of Malibu, Calif.

Philips Medical Systems: Easy Access Software releases 1.1, 5.2, 6.2 & 7.2

If DICOM fields for body part, description or accession number are changed, change won't update on the EasyWeb client or hospital systems.

FDAJun 27, 2003Nationwide• Philips Medical Systems

Cosco Arriva Infant Car Seats (Dorel) – Child Safety Concern (2003)

The recalled car seats/carriers were sold under the Cosco Arriva and Turnabout brand names and were manufactured by Dorel Juvenile Group in the U.S. The car seat/carriers have the following model numbers: ARRIVA 02-665 02-727 02-728 02-729 02-731 02-732 02-733 02-750 02-751 02-755 02-757 02-774 TURNABOUT 02-753 02-756 02-758 02-759 02-760 02-761 02-762 02-763 02-764 02-765 02-770 02-771 02-772 The model number and manufacture date are located on the instruction and warning label on the side of the car seat/carrier. The recalled seats were manufactured on or before Jan. 31, 2000.

CPSCJun 25, 2003Nationwide• Dorel Juvenile Group Inc., of Columbus, Ind.

Ski-Doo Snowmobiles (Bombardier) – Vehicle Safety Issue (2003)

Laceration Risk

The recalled snowmobiles are 2-tone blue or all black. The name of the engine is written on the hood: Rotax 4-TEC V-1000 or Rotax 2-TEC 800 SDI.

CPSCJun 24, 2003Nationwide• Bombardier Motor Corporation of America, of Grant, Fla.

Beckman Coulter Inc: Power Processor Aliquot Tube Labels Part 800255

Labels are missing an expiration date and storage instructions, increasing the likelihood that they will not be used by the expiration date or may be stored under conditions that would cause adhesive failure and loss of identity of sample or aliquot during testing.

FDAJun 23, 2003Nationwide• Beckman Coulter Inc

Misys Healthcare Systems: Misys Laboratory System versions5.3 up to 5.3.2 with LabA...

Software defect. When Quality Assurance failure warnings are missing from a patient's report abnormal results could be used for diagnosis or treatment.

FDAJun 23, 2003Nationwide• Misys Healthcare Systems

Beckman Coulter Inc: Synchron LX Systems Primary Tube Sample Template (a piec...

Dead volume on sight gauge for the Synchron LX 20 and LX 20 Pro Systems not stated, which may result in instrument error.

FDAJun 19, 2003Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: Access Immunoassay System Technical Update 03.1, Part num...

Defective software media distributed with upgrade software may cause installation failure and systems lock.

FDAJun 18, 2003Nationwide• Beckman Coulter Inc