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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 3581–3600 of 3680 recalls

Philips Medical Systems Sales & Service Region No. America: Diagnost 96

Potential for table to move by itself

FDAAug 10, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Terumo Cardiovascular Systems Corp: Sarns brand Retrograde Cardioplegia Cannula, 17 Fr, steer...

Product is labeled as sterile, but inadequate package seal results in lack of assurance of sterility.

FDAAug 8, 2003Nationwide• Terumo Cardiovascular Systems Corp

Stryker Howmedica Osteonics: T2 Tibia Nail, Standard 9 x 300 mm, T2 Tibia System, Cat...

The device does not have an oblong hole for dynamic locking as required.

FDAAug 4, 2003CA, GA, IN +3 more• Stryker Howmedica Osteonics

1...178 179180181 182...184

Page 180 of 184Next

American Medical Systems: Monarc Subfascial Hammock With Tensioning Suture, Product...

Insertion needles from the former version of the product were packaged with the new sling with dilator that is different than the old version and not compatible with the old needles.

FDAJul 28, 2003Nationwide• American Medical Systems

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, 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

Stryker Howmedica Osteonics: Femoral Resection Guide, Scorpio L.R.S. Instrumentation.

Scorpio Femoral Resection Guides have the potential to remove more bone than necessary.

FDAJul 17, 2003IN• Stryker Howmedica Osteonics

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

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

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

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

Misys Healthcare Systems: Misys Laboratory System, versions 5.2, 5.23 and 5.3

Software anomally Results with a global flag failure that autofile without review can cause abnormal results being communicated without associated abnormal designations.

FDAJun 10, 2003Nationwide• Misys Healthcare Systems

Trisonic Nightlights – Electrical Safety Concern (2003)

Fire/Burn Risk

The recalled nightlights have a yellow exterior shaped like a smiley face. A label on the back of the nightlight reads, "Trisonic, 4W/120V custom made in China for Trisonic, Queens, NY, TS-45431."

CPSCJun 5, 2003Nationwide• Trisonic/Eastern America Trio Products, of Flushing, N.Y.

Misys Healthcare Systems: Misys Laboratory System using Microbiology versions 5.2 (...

Susceptibility comments are ommited from Microbiology cumulative reports

FDAJun 2, 2003Nationwide• Misys Healthcare Systems

Coapt Systems, Inc.: Drill bits used in ENDOTINE Forehead 3.5 and 3.0, Catalog...

During use, the device has a potential for unacceptable deep hole in the cranium which can cause patient injury.

FDAMay 23, 2003OR• Coapt Systems, Inc.