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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

893

Class I (Serious)

124

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 15321–15340 of 17593 recalls

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

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.

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FDA

Aug 7, 2008

Nationwide

• Smith And Nephew, Inc. Wound Management Division

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.

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.

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

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

Medtronic Inc. Cardiac Rhythm Managment: Maximo II CRT D284TRK, for ventricular pacing and defibri...

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

J T Posey Company: Posey Synthetic Leather and Biothane Waist and Wrist Rest...

Failure to restrain: This recall was initiated after a complaint was received by the firm regarding a Posey 2217SL unit indicating that a patient was able to pull the rivet or washer through the synthetic leather allowing the patient to have freedom of arm movement. A second complaint was received indicating that a patient was able to tear the strap at the adjustment notch on a Posey 221 7SL unit

FDAJul 25, 2008Nationwide• J T Posey Company

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo II DR D28DRG, for ventricular pacing an...

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

Reebok Studio Exercise Cycles – Laceration Risk (2008)

Laceration Risk

The Reebok Studio Cycle is an upright exercise bike used primarily in fitness centers and other institutional settings. The recalled bicycle is black with silver cranks. The unit has an internal belt drive. The base of the bicycle is a single piece that is welded to the frame. The legs are two straight horizontal bars with rounded edges. There is a logo located on the side of the exercise cycle that shows a person riding a bicycle.

CPSCJul 24, 2008Nationwide• Fitness Associates Incorporated (F.A.I.), under license from Reebok International Ltd., of Canton, Mass. Note: F.A.I. is no longer in business.

Dirt Devil Power Brush Attachment – Laceration Risk (2008)

Laceration Risk

The recalled Dirt Devil Turbo Tool/Power Brush attachment was sold as an accessory with the following Dirt Devil vacuum models. Only vacuum tool accessories with date codes J7060 through J7365 and have a C-clip connector are included in this recall. The date code is located on the underside of the vacuum accessory. The Turbo Tool/Power Brush tools are about 6 ½ inches long by about 5 inches wide and come in a variety of colors that match the color of the vacuum. The housing of the tool was made in clear, red, green, or light blue with clear, light blue, dark blue, red, purple, or black turbine fans with matching brush rolls. Dirt Devil Vacuum Models Reaction Purpose for Pets Ultra Swivel Glide M110000 M140000 M086020 M110000HD M140000CA M110001B M110002 Envision Wide Glide Swerve M110003 M086700WCA M086030 M110006 M086710 M086030CA M110008 M110008CA Action Upright Royal Commercial M110009 M110020CAB RY6100

CPSCJul 23, 2008Nationwide• TTI Floor Care North America, of Glenwillow, Ohio

Walther Air Pistol Cylinders – Burst Risk (2008)

The recalled Walther air cylinders for air pistols are aluminum and involve model 2/WALTHER 85 cm3, with the imprinted test date between 6 00 and 6 01 2000/2001 located on the end of the cylinder.

CPSCJul 23, 2008Nationwide• Carl Walther GmbH, Sportwaffen, of Germany

Philips Medical Systems: Philips Telemonitoring System Software (M3811B) used with...

Software: If Weight Limits edited, values will return to default values that were deleted

FDAJul 22, 2008Nationwide• Philips Medical Systems

BD Diagnostics (GeneOhm Sciences, Inc): BD GeneOhm MRSA 200 ct, Catalog #441242. IDI-MRSA assay...

BD Diagnostics GeneOhm (BDDG) initiated the recall after they identified that the product has the potential to identify a patient as falsely positive for colonization with methicillin resistant Staphylococcus aureus. The potential health hazard related to a false positive result from this assay would be that a patient may be misclassified as having MRSA colonization when in fact they do not have

FDAJul 21, 2008Nationwide• BD Diagnostics (GeneOhm Sciences, Inc)

BD Diagnostics (GeneOhm Sciences, Inc): BD GeneOhm MRSA 48 ct, Catalog #441244. IDI-MRSA assay i...

FDAJul 21, 2008Nationwide• BD Diagnostics (GeneOhm Sciences, Inc)

Terumo Cardiovascular Systems Corporation: Terumo Advanced Perfusion System 1 base, 110/120V; Model ...

Local pump controls including start/stop button, select button and manual button may not function.

FDAJul 18, 2008Nationwide• Terumo Cardiovascular Systems Corporation

Terumo Cardiovascular Systems Corporation: Terumo Advanced Perfusion System 1 base; Model 801764. N...

The units may exhibit blank or distorted displays, loss of local control and/or may have local control knobs that are difficult to use.

FDAJul 18, 2008Nationwide• Terumo Cardiovascular Systems Corporation

Terumo Cardiovascular Systems Corporation: Terumo Advanced Perfusion System 1 Base, 100/120V; Model ...

The pumps may exhibit blank or distorted displays, loss of local control and/or may have local control knobs that are difficult to use.

FDAJul 18, 2008Nationwide• Terumo Cardiovascular Systems Corporation

Terumo Cardiovascular Systems Corporation: Terumo Advanced Perfusion System 1 (4 inch diameter Rolle...

Overspeed and underspeed errors, erratic pump behavior, jerky operation at low RPMs, pump instability, pump slowdowns and pump stops due to overspeed max events may occur due to a grease leak onto the motor speed encoder disk.

FDAJul 18, 2008Nationwide• Terumo Cardiovascular Systems Corporation