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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

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 10741–10760 of 10937 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

Becton Dickinson & Company: BD Blood Glucose Test strips. BD Latitude, 100 Test Stri...

Test Strips may not be meeting specifications at the lower range of glucose values.

FDAJul 23, 2003Nationwide

1...536 537538539 540...547

Page 538 of 547Next

• Becton Dickinson & Company

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, 2003Nationwide• 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

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.

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.

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

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.

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

Misys Healthcare Systems: Misys Laboratory System versions 5.3 up to 5.3.2 with Ana...

Software anomaly allows patient reports to contain incomplete data used for diagnosis or treatment.

FDAJun 16, 2003Nationwide• Misys Healthcare Systems

Ohmeda Medical, A division of Datex-Ohmeda, Inc.: Servo Controlled Oxygen System for Ohmeda''s Medical Gira...

Firm's received complaints of medical device malfunction affecting instrument's calibration and alarm systems.

FDAJun 13, 2003Nationwide• Ohmeda Medical, A division of Datex-Ohmeda, Inc.