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Varian Medical Systems Oncology Systems

Varian Medical Systems Oncology Systems Recalls

All product recalls associated with Varian Medical Systems Oncology Systems.

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Recall Summary

Total Recalls

1000

Past Year

1000

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 17681–17700 of 21320 recalls

Varian Medical Systems Oncology Systems: Eclipse 8.5 (build 8.2.2X) systems with distributed Calcu...

When using the multiple static segment option, the device may alter dose delivery.

FDAOct 2, 2008Nationwide• Varian Medical Systems Oncology Systems

Philips Medical Systems North America Co. Phillips: Nuclear Magnetic Resonance Imaging System (MRI). Trace it...

Fire/Burn Risk

The cables of the coil may become too hot and cause burns when placed too close to the patient. While using the 1.5T Sense XL Torso coil, unwanted radiofrequencies (RF) interaction with the patient can occur. Especially in combination with high SAR levels and when the RF cables of the coil are too close to the patient, this RF interaction has resulted in RF burns to patients.

FDASep 30, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Varian Medical Systems, Inc.: GammaMed Plastic Needle with Mandrin; 2.0 mm diameter, le...

1...883 884885886 887...1066

Page 885 of 1066Next

Plastic needle tip could possibly crack or separate.

FDASep 30, 2008Nationwide• Varian Medical Systems, Inc.

Regenesis Biomedical Inc: Regenesis Biomedical PROVANT Wound Therapy System, Model ...

In the course of device testing, the firm determined that the affected devices may, under certain unusual clinical circumstance, be unable to generate a therapeutic dose of radio frequency energy. As such, for these few devices, the effectiveness of Provant therapy may be impaired.

FDASep 29, 2008NC, VA, WY• Regenesis Biomedical Inc

Toshiba American Medical Systems Inc: Toshiba Infinix fluoroscopy DFP-8000D Digital Radiography...

Audible signal is not available at all times when using the HLC fluoroscopy mode. Special means of activation are not designed in for selection of High Level Controls, as required by regulation.

FDASep 29, 2008Nationwide• Toshiba American Medical Systems Inc

Rockwell Medical Technologies, Inc: SteriLyte Liquid Bicarbinate, Formula CL-02; 1 gallon (3....

Microbial growth was observed in the retain samples of 4 lots of Liquid Bicarbonate after products had been distributed.

FDASep 29, 2008Nationwide• Rockwell Medical Technologies, Inc

Medtronic Cardiovascular Revascularization & Surgical Therap: DLP(R) Pericardial/Intracardiac Sump Cannulae, 20 Fr., P/...

Separates: Six complaints were received from two locations. In all cases the sump tip assembly separated from the tubing during device removal and had to be retrieved from the patient. There were no adverse events affecting these patients.

FDASep 29, 2008IL, IN, IA +6 more• Medtronic Cardiovascular Revascularization & Surgical Therap

Siemens Medical Solutions USA, Inc.: Symbia T16 System; a dual-detector variable angle gamma c...

The protective plastic cap over the CT gantry power switch on the Line Connection Box may come loose, exposing the energized electrical contacts within the switch, thereby causing an electric hazard.

FDASep 29, 2008Nationwide• Siemens Medical Solutions USA, Inc.

Siemens Medical Solutions USA, Inc.: Symbia T6 System; a dual-detector variable angle gamma ca...

The protective plastic cap over the CT gantry power switch on the Line Connection Box may come loose, exposing the energized electrical contacts within the switch, thereby causing an electric hazard.

FDASep 29, 2008Nationwide• Siemens Medical Solutions USA, Inc.

Bd Diagnostic Systems Tripath: BD PrepStain System, Model Number: 799-14000-00; Catalog ...

Software Error in the non-gyn program of some devices may cause non-gyn samples to be incorrectly transferred from centrifuge tubes to slides potentially result in mismatched patient results.

FDASep 26, 2008Nationwide• Bd Diagnostic Systems Tripath

Genico, Inc., dba Genicon: Genicon 5mm Pyramidal Trocar, Sterile, Genion 6869 Stapoi...

The stainless steel tips on the Genicon 5mm Pyramidal Trocar exhibited contamination that resembled rust and there was also pitting on the tip of the trocar.

FDASep 25, 2008Nationwide• Genico, Inc., dba Genicon

Hologic, Inc.: Hologic, Inc., 10 Year Fracture Risk Questionnaire Option...

Software error may lead to a high estimate of major fracture probability.

FDASep 24, 2008Nationwide• Hologic, Inc.

ela Medical Llc: Sorin Group Reply DR Rate responsive dual-chamber pacemak...

Analysis showed that the screwdriver was not fully inserted in the setscrew's hex cavity, which damaged the setscrew.

FDASep 23, 2008Nationwide• ela Medical Llc

Philips Medical Systems (Cleveland) Inc: Vertical drive brake (on patient supports). Used on cer...

The product is being recalled because the patient support may travel downwards without being commanded to move.

FDASep 23, 2008AL, AK, AZ +41 more• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: Respiratory Gating System which includes: Pulmonary Digit...

Images not correlated: A leak between the Tube Interface and the Outlet Tube of the transducer may result in a failure to produce respiratory correlated images.

FDASep 22, 2008PR• Philips Medical Systems (Cleveland) Inc

Trek Diagnostic Systems: HARDY DIAGNOSTIC McFarland Standard 0.5; in vitro diagnos...

Incorrect result: The absorbance has changed as the standards have aged; the standards' turbidity has become denser. The recalled lot is now reading 0.15 ABS @ 625 nm. TREK'S internal specification and the manufacturer's (Hardy Diagnostics) specification is 0.08 - 0.10 ABS @625 nm. CLSI specifies 0.08 - 0.13 ABS @ 625 nm.

FDASep 22, 2008IL, IN, OH• Trek Diagnostic Systems

Advanced Bionics Corp: Precision Charger 1.0 (Model Number SC-5300) for the Prec...

Fire/Burn Risk

Since April 2004, 27 of 8,769 (0.31%) patients have reported receiving second degree burns in the area of charging and 3 of 8,769 (0.03%) patients have reported receiving third degree burns in the area of charging while using Charger 1 .0. Some of these events were the direct result of the patient disregarding the instructions for use, such as sleeping with the Charger on or placing it directly on

FDASep 22, 2008Nationwide• Advanced Bionics Corp

Hologic, Inc.: ATEC Breast Biopsy and Excision System 12 gauge, 20 centi...

The distal tip of the needle may become detached and remain in the patient, requiring surgical removal.

FDASep 22, 2008Nationwide• Hologic, Inc.

Respironics California Inc: Respironics BiPAP Focus Noninvasive Ventilator System. T...

Power Supply failures have occurred on some ventilators. A discrepancy between the power supply strain relief clip and the power cord connector may allow unwanted movement of the cord and the unit's power supply. A disconnection or intermittent electrical connection between the power cord and the unit's power supply during operation or charging can result in transient power surges, which may cau

FDASep 22, 2008Nationwide• Respironics California Inc

CAS Medical Systems, Inc.: CASMED 500cc Unifusor Classic with piston gauge and thumb...

Leaks: Infusion Cuffs may exhibit air leakage at the union of the tube and bag, and not maintain pressure. For further information, please contact the firm at 203-488-6056.

FDASep 20, 2008Nationwide• CAS Medical Systems, Inc.