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Philips Medical Systems

Philips Medical Systems Recalls

All product recalls associated with Philips Medical 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 22561–22580 of 25000 recalls

Philips Medical Systems: Philips Diagnostic Ultrasound System, Model HD3. Product...

The system has a software defect that affects the display of Estimated Fetal Weight (EFW) Growth Percentile result values.

FDAAug 12, 2008PR• Philips Medical Systems

OEC Medical Systems, Inc: GE OEC 9900 Elite Fluoroscopic X-Ray System, GE Healthcar...

Beam limitation may be non-compliant on some X-ray units.

FDAAug 12, 2008Nationwide• OEC Medical Systems, Inc

OEC Medical Systems, Inc: GE OEC 9800 Fluoroscopic X-Ray System, GE Healthcare, Sur...

Beam limitation may be non-compliant on some X-ray units.

FDAAug 12, 2008Nationwide• OEC Medical Systems, Inc

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Varian Medical Systems Oncology Systems: Exact Couch with Exact Couch Top, a component of the C-Se...

During couch movement, a patient's fingers may get pinched at certain points which could result in broken, disengaged or pinched fingers.

FDAAug 11, 2008Nationwide• Varian Medical Systems Oncology Systems

Nova Biomedical Corporation: Stat Profile Critical Care Xpress (CCX and CCX+), CCX Cre...

Erroneous, low creatinine results on CCX analyzer

FDAAug 11, 2008Nationwide• Nova Biomedical Corporation

Philips Medical Systems: Philips HeartStart FRx Defibrillator, Automated External ...

The affected device may not deliver appropriate defibrillation therapy.

FDAAug 7, 2008Nationwide• Philips Medical Systems

Smith And Nephew, Inc. Wound Management Division: GlobTek, Inc. Power Supply for Medical Use Part No: TR9CE...

External battery chargers used with the Version 29 VISTA Negative Pressure Wound Therapy pumps are failing to properly charge the pump's battery.

FDAAug 7, 2008Nationwide• Smith And Nephew, Inc. Wound Management Division

Navilyst Medical: NAMIC Custom Angiographic Kit, Right Heart Kit, REF/Catal...

Firm became aware that a specific batch of the product may contain loose plastic particulates in the fluid pathway.

FDAAug 6, 2008MO• Navilyst Medical

Varian Medical Systems, Inc.: GammaMed Flexible Applicator Probe, Part GM11002560 - 3....

GammaMed Flexible Applicator Probes may not have been heat annealed during manufacturing to prevent shrinkage after autoclave.

FDAAug 5, 2008Nationwide• Varian Medical Systems, Inc.

Greiner Bio-One North America, Inc.: Plastic Cannula Holdex Tube Holder, Item number: 450216. ...

At removal of the tube from the holder the needle may dislodge and become stuck in the tube stopper with the blunt end of the needle facing out.

FDAAug 5, 2008AL, FL, IN +13 more• Greiner Bio-One North America, Inc.

Cordless Brad Nailers (DEWALT) - Injury Hazard (2008)

This recall involves the DEWALT DC608 18-Volt Cordless 2" 18-Gauge Straight Brad Nailer with date codes 200728 through 200821. "DC608" is located on the right side of the magazine. The date code can be found on the underside of the handle, once the battery pack is removed. Units stamped with an "M" following the date code are not included in this recall.

CPSCAug 5, 2008Nationwide• DEWALT Industrial Tool Co., of Towson, Md.

Animas Corporation: One Touch Ping Glucose Monitoring System Combines the fu...

display old, inaccurate values for bolus amount delivered and amount of planned bolus totals

FDAAug 4, 2008Nationwide• Animas Corporation

Animas Corporation: Battery Caps used with OneTouch Ping Glucose Monitoring S...

Unintentional rebooting: Pump products exhibit an intermittent loss of power due intermittent loss of contact between battery cap and battery canister resulting in the device resetting. The failure of the battery cap may result in failure of the device to administer insulin therapy which may result in hyperglycemia.

FDAAug 4, 2008AR, CA, FL +10 more• Animas Corporation

Animas Corporation: Battery Caps used with Animas 2020 Insulin Pump. The pum...

FDAAug 4, 2008AR, CA, FL +10 more• Animas Corporation

Animas Corporation: Battery Caps used with insulin pumps and glucose monitori...

FDAAug 4, 2008AR, CA, FL +10 more• Animas Corporation

Immunodiagnostics Systems Inc: IDS 25-Hydroxy Vitamin D EIA Enzymeimmunoassay for the qu...

A small number of customers have experienced low absorbance values when using kits from this batch.

FDAAug 2, 2008Nationwide• Immunodiagnostics Systems Inc

Sunquest Information Systems, Inc.: Sunquest Laboratory System. Software Version: Sunquest ...

While performing in-house testing for the Sunquest Laboratory System and under certain conditions, there have been instances in which an error that occurred at the database level or originated in the operating system (Cache)was not communicated or displayed in the Graphic User Interface (GUI) application so the activity continued. While this error was registered in the error log in the System U

FDAAug 1, 2008Nationwide• Sunquest Information Systems, Inc.

Climbing Ropes (New England) - Fall Hazard (2008)

Two types of climbing ropes have been included in this recall, the Maxim Apogee 9.1mm and Maxim Pinnacle 9.5mm. The Maxim Apogee 9.1mm is a 48 carrier climbing rope. The colors are yellow and black, and red and yellow. The model numbers are 3411-91 and 3415-91, with date codes 060801 thru 080601. The UPC codes are: 75396312299, 75396312298, 75396312301, and 75396312300. The Maxim Pinnacle 9.5mm is a blue 48 carrier climbing rope. The Model number is 3403-95, with date codes 070201 thru 080601. The UPC codes are 75396312292 and 75396312293. The date codes and the UPC codes are on the original packaging.

CPSCJul 29, 2008Nationwide• New England Ropes, of Fall River, Mass.

Greiner Bio-One North America, Inc.: VACUETTE, 2 ml Lithium Heparin Venous Blood Collection Tu...

Labeling Error: Incorrect tube label reads "Z Serum Clot Activator" instead of "LH Lithium Heparin" tube. All other information on the tube label including color coding of tube was correct. Case and rack label information showed the correct information with 2 ml Lithium Heparin.

FDAJul 29, 2008AL, AK, AR +30 more• Greiner Bio-One North America, Inc.

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo II VR D284VRC, for ventricular pacing an...

Maximo II VR ICD, DR ICD and CRT-D inadvertently include the Capture Management algorithm (Atrial/Right Ventricular/Left Ventricular Capture management). The Capture management algorithm monitors daily pacing thresholds and may increase or decrease pacing amplitudes in response to patients' needs. Although the algorithm is operating correctly, it is not accessible to the clinician for reprogramm

FDAJul 25, 2008Nationwide• Medtronic Inc. Cardiac Rhythm Managment