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Ventana Medical Systems Inc

Ventana Medical Systems Inc Recalls

All product recalls associated with Ventana Medical Systems Inc.

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Recall Summary

Total Recalls

1000

Past Year

583

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 9701–9720 of 10937 recalls

Ventana Medical Systems Inc: Ventana Image Analysis System (VIAS) - PATHWAY anti-HER-2...

Incomplete upgrade: The software upgrade from February 1, 2007 may not have been completed. This software upgrade adds the algorithm (Slidetype) for the PATHWAY anti-HER-2/neu (4B5) antibody to the VIAS system.

FDAJun 26, 2007Nationwide• Ventana Medical Systems Inc

Varian Medical Systems Inc: Ximatron Digital Imaging (Ximavision), V 7.5.51 with Serv...

Unexpected loss of Treatement Field Add-Ons (Wedges, Blocks, etc) during Ximatron simulation. If an unapproved treatment field is created without an MLC, but with an add-on, the add on will be deleted without warning. If this is not detected and corrected, incorrect dose delivery will occur.

FDAJun 25, 2007MO, NY• Varian Medical Systems Inc

Medtronic Neuromodulation: Medtronic InterStim INS (Model 3023) with N'Vision Inter ...

Software issue may cause false low battery alert to be displayed when interrogating an Interstim Implantable Neurostimulator (Model 3023) with an N'Vision Clinician Programmer (Model 8840), or with an Inter Stim iCon Patient Programmer (Model 3037).

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FDAJun 25, 2007Nationwide• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic InterStim II INS Model 3058 with N'Vision Inter...

A software issue may cause a lower than expected battery capacity estimate when evaluating an InterStim II Implantable Neurostimulator (model 3058) with an N'Vision Clinician Programmer(Model 8840) before implant .

FDAJun 25, 2007Nationwide• Medtronic Neuromodulation

Becton Dickinson & Company: ReliOn 0.5cc 30 g x 8mm Blister Pak U-100 syringe 30 gaug...

Complaints received indicating open seals on blister paks, potentially compromising the sterility of the product.

FDAJun 21, 2007Nationwide• Becton Dickinson & Company

Polaris Outlaw 525 ATVs (Polaris) – Fire Hazard (2007)

Fire/Burn Risk

The recall involves 2007 model year Polaris "Outlaw 525" ATVs. They are available in black or white.

CPSCJun 20, 2007Nationwide• Polaris Industries Inc., of Medina, Minn.

Applied Composite Technology: VS-1000 Senator Prosthetic Foot, (Categories 5 and 6, siz...

Prosthetic foot device may loosen or separate during use; due to structural inconsistency that may cause a pyramid failure.

FDAJun 20, 2007CA, CO, FL +14 more• Applied Composite Technology

Stationary Gas/Propane Generators (Cummins) – Fire Hazard (2007)

Fire/Burn Risk

The recall involves both commercial and residential model Cummins Power Generation gaseous-fueled stationary generator sets (fueled by propane or natural gas). They have the following model numbers listed on the generator nameplate which is located at the front base of the unit: commercial models GGDB, GGMA/B/C, and GNAA/B/C, and residential models RS15000, RS20000, and RS30000. These units also have serial number A050734102 through L068998479 and "Cummins Power Generation" listed on the generator nameplate.

CPSCJun 19, 2007Nationwide• Cummins Power Generation Inc., of Fridley, Minn.

Smiths Medical MD, Inc.: Smiths CADD Yellow Medication Cassette Reservoir, With cl...

Smith Medical has become aware that an increase in pH may occur with some medications when instilled in the Affected Cassettes. Also, a small number of catheter occlusions have been reported from one customer when these Affected Cassettes have been used for delivering Flolan.

FDAJun 18, 2007PR• Smiths Medical MD, Inc.

Smiths Medical MD, Inc.: Smiths CADD Medication Cassette Reservoir, With clamp and...

FDAJun 18, 2007PR• Smiths Medical MD, Inc.

Medtronic Emergency Response Systems, Inc.: biphasic LIFEPAK 500 automated external defibrillators (A...

Reduced Shock- the device may deliver 100 Joule (J) to a patient, which is less than the recommended factory minimum default setting of 200 J.

FDAJun 13, 2007Nationwide• Medtronic Emergency Response Systems, Inc.

GE OEC Medical Systems, Inc: GE OEC 6800 Fluoroscopic X-ray System, GE Healthcare, Sal...

X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.

FDAJun 12, 2007CO, FL, GA +4 more• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC 8800 Fluoroscopic X-ray System, GE Healthcare, Sal...

X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.

FDAJun 12, 2007CO, FL, GA +4 more• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC 9800 Fluoroscopic X-ray System, GE Healthcare, Sal...

X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.

FDAJun 12, 2007CO, FL, GA +4 more• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC 2800 mobile Fluoroscopic X-ray System, GE Healthca...

X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.

FDAJun 12, 2007CO, FL, GA +4 more• GE OEC Medical Systems, Inc

Globe Model J Dry Fire Sprinklers – potential failure (2007)

Fire/Burn Risk

Model J Series dry fire sprinklers come in pendent, upright, and sidewall configurations. The name "Globe," the letter "J" and the year of manufacture (1990 though 1999) are embossed on the frame of each sprinkler. These dry sprinklers were designed to be installed in areas of buildings where the sprinklers or water supply pipes may be subject to freezing, such as unheated attics, freezers and coolers, parking garages, porches and warehouses.

CPSCJun 12, 2007Nationwide• Globe Fire Sprinkler Corp., of Standish, Mich.

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

X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.

FDAJun 12, 2007CO, FL, GA +4 more• GE OEC Medical Systems, Inc

Philips Medical Systems: Philips Medical HeartStartXL Defibrillator/Monitor Model ...

The ECG signal may become unusable to assess patient condition and need for therapy.

FDAJun 11, 2007Nationwide• Philips Medical Systems

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: BrainLAB Target Positioner for Leksell Headring used with...

Target Alignment Error : A mechanical component/software incompatibility caused by a specific combination of the BrainLAB Target Positioner version 40700-3A for Leksell headrings and BrainLAB planning software resulted in a 1.25 mm shift in target area alignment during radiosurgery treatment.

FDAJun 5, 2007OH, WA• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Smiths Medical PM, Inc.: BCI Advisor Vital Signs Monitor (Model/Catalog Number: 9200)

Turn off unexpectedly/ Not turn on : monitors turned off unexpectedly sounding the critical failure alarm. Advisor Vital Signs monitors that were off, would not turn back on.

FDAJun 5, 2007PR• Smiths Medical PM, Inc.