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Misys Healthcare Systems

Misys Healthcare Systems Recalls

All product recalls associated with Misys Healthcare Systems.

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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 24541–24560 of 25000 recalls

Misys Healthcare Systems: Calculator/ Data Processing Module for Clinical Use

Software Design Defect. Under certain conditions, results are removed.

FDAJul 24, 2003Nationwide• Misys Healthcare Systems

Misys Healthcare Systems: Calculator/ Data Processing Module for Clinical Use

Software Defect. Data used in the diagnosis and or treatment of a patient's illness are missing from the patient result report.

FDAJul 23, 2003Nationwide• Misys Healthcare Systems

Misys Healthcare Systems: Misys Laboratory System versions 5.2 through 5.3.2 using ...

Software design deficiency. If the dilution factor is added to the same result twice, incorrect specimen values are reported.

FDAJul 22, 2003

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Nationwide

• Misys Healthcare Systems

Misys Healthcare Systems: Misys Laboratory System, versions 5.3 build 63 through 5....

Incorrect demographics display which can result in incorrect information being used in diagnosis or treatment of patients.

FDAJul 21, 2003Nationwide• Misys Healthcare Systems

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

Slow Cookers (Hamilton Beach) – Electrical Safety Risk (2003)

Fire/Burn Risk

The recalled slow cookers were sold under the Hamilton Beach and Proctor-Silex brand names, which are printed on the front of the base of the unit. The slow cookers are either round or oval, and were sold in solid white and various print designs. They have a capacity of 3.5 to 6.5 quarts. The slow cookers have series codes A through D which are printed on the bottom along with the model number. Brand Names Model Numbers Hamilton Beach 33390, 33475, 33575, 33590, 33675, 33690, 33725, 33850, 33860 Hamilton Beach / Portfolio 33680 Proctor-Silex 33320, 33320FD, 33325, 33375, 33380, 33625A

CPSCJul 17, 2003Nationwide• Hamilton Beach/Proctor-Silex, of Glen Allen, Va.

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."

CPSCJul 17, 2003Nationwide• 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.

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.

Allergan Medical Optics Inc: AMO PhacoFlex II Model SI40NB, Intraocular Lenses

Post operative complaints of cloudiness in the intraocular lenses.

FDAJul 2, 2003Nationwide• Allergan Medical Optics Inc

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.

Egg Dippers Easter Plush Toys (Small Small World) – Toy Safety Issue (2003)

The recall includes four animal plush toys. The white rabbit has a purple egg which reads "Happy Easter," the green rabbit has a yellow egg which reads "Happy Easter," the purple bear has a purple egg which reads "Happy Easter," and the yellow duck carries a green egg which reads "You're Egg-stra Special." Each toy has a permanent label affixed which reads "The Boyd's Collection, Ltd."

CPSCJul 2, 2003Nationwide• Small Small World, of Englewood, N.J.

Kawasaki KFX700 V-Force ATVs (Kawasaki) – Vehicle Safety Problem (2003)

The Kawasaki KFX700 "V-Force" is a four-wheel ATV with a variable automatic transmission. The green or orange ATVs have "Kawasaki," "KFX700" and "V-Force" written on them.

CPSCJun 30, 2003Nationwide• Kawasaki Motors Corp., U.S.A., of Irvine, Calif.