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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)

91

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 9941–9960 of 10937 recalls

Ventana Medical Systems Inc: Discovery, Slide Staining System, Catalog Number: N750-DI...

Leaking Carboys/Safety Updates:The Ventana Staining Platform includes one or more carboys that may have the potential to leak if the spigot is either improperly installed or not fully closed.

FDASep 29, 2006Nationwide• Ventana Medical Systems Inc

Ventana Medical Systems Inc: Benchmark LT, Slide Staining System, Catalog Number: N750...

Leaking Carboys/Safety Updates:The Ventana Staining Platform includes one or more carboys that may have the potential to leak if the spigot is either improperly installed or not fully closed.

FDASep 29, 2006Nationwide• Ventana Medical Systems Inc

Ventana Medical Systems Inc: Benchmark, Slide Staining System, Catalog Number: N750-BM...

Leaking Carboys/Safety Updates:The Ventana Staining Platform includes one or more carboys that may have the potential to leak if the spigot is either improperly installed or not fully closed.

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FDASep 29, 2006Nationwide• Ventana Medical Systems Inc

Ventana Medical Systems Inc: Discovery XT, Slide Staining System, Catalog Number: N75...

Leaking Carboys/Safety Updates:The Ventana Staining Platform includes one or more carboys that may have the potential to leak if the spigot is either improperly installed or not fully closed.

FDASep 29, 2006Nationwide• Ventana Medical Systems Inc

Ventana Medical Systems Inc: Benchmark XT, Slide Staining System, Catalog Number: N750...

Leaking Carboys/Safety Updates:The Ventana Staining Platform includes one or more carboys that may have the potential to leak if the spigot is either improperly installed or not fully closed.

FDASep 29, 2006Nationwide• Ventana Medical Systems Inc

Smiths Medical MD, Inc.: Locator-Wand Cover that is sold in a shelf carton (unit p...

Smiths Medical became aware that product returned to them under recall # Z-0800-06/ Z-0807-06 was inadvertently distributed to consignees after the recall was initiated 03/29/2006. The product was originally recalled because Locator Wand covers, which are supplied on the outside of PORT-A-CATH and P.A.S. PORT sterile trays, may have an insufficient seal and product sterility could be compromised.

FDASep 27, 2006CA, FL, MD +4 more• Smiths Medical MD, Inc.

ICU Medical, Inc.: Orbit 90 Subcutaneous Infusion Set, 9 mm Catheter, 42" Tu...

The product contains a female luer which has been reported to crack in use allowing fluid to leak from the device.

FDASep 26, 2006CA, GA, OH +2 more• ICU Medical, Inc.

Varian Medical Systems Inc: 4D Integrated Treatment Console and Varis 1.4g Medical Ch...

Selecting an empty space next to the ''Override'' or ''Acquire Actual'' buttons may result in mistreatment to the patient.

FDASep 21, 2006Nationwide• Varian Medical Systems Inc

Philips Medical Systems: M3001A Philips Multi Measurement Server (MMS)

Unexpected pulse oximetry (Sp02) readings (100%) over time when a sensor is not attached to the patient. In addition, with a sensor attached to a patient, an incorrect high Sp02 may be displayed when a pulse rate is in a range of 185BPM

FDASep 21, 2006Nationwide• Philips Medical Systems

Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342: Advanced Bionics Precision Linear Leads, part of the Prec...

A small number of unimplanted Precision Linear Leads may have been assembled with incorrect electrode material. At high stimulation levels, the metal may corrode and dissolved metals may enter the patient.

FDASep 21, 2006Nationwide• Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342

Philips Medical Systems: M1020B PulseOximetry Module Philips FAST Sp02 and Pulse O...

Unexpected pulse oximetry (Sp02) readings (100%) over time when sensor is not attached to patient. In addition, with a sensor attached to a patient, an incorrect high Sp02 may be displayed when a pulse rate is in a range of 185BPM

FDASep 21, 2006Nationwide• Philips Medical Systems

Arctic Cat Snowmobile – Steering Failure (2006)

The recalled steering shafts were installed on the following models: All 2002 440 Sno Pro Models All 2003 Firecat 500/600/700, Firecat 700 Sno Pro, and 440 Sno Pro Models All 2004 Firecat 500/600/700 (STD and Sno Pro), and Sabercat 500/600/700 Models All 2005 Firecat 500/600/700 (STD and Sno Pro), M5,M6,M7, and Sabercat 500/600/700 Models All 2006 Crossfire 600/700, Firecat 500/600/700, Firecat 700 Sno Pro, Sabercat 500/600/700, and all M-Series

CPSCSep 19, 2006Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

GE OEC Medical Systems, Inc: InstaTrak with Multiple Dataset Navigation, 892.2050 Syst...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. On October 11, 2006, GE Healthcare recalled GE OEC InstaTrak 3500 Plus System with Software version 5.2, the surgical Navigation and Visualization Application due to software related issues.

FDASep 15, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: InstaTrak with Multiple Dataset Navigation, 892.2050 Syst...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. On October 11, 2006, GE Healthcare recalled GE OEC InstaTrak 3500 Plus System with Software version 5.2, the surgical Navigation and Visualization Application due to software related issues.

FDASep 15, 2006Nationwide• GE OEC Medical Systems, Inc

Michigan Instruments, Inc.: Michigan Instruments Thumper Mechanical CPR Device; Model...

Failure to initiate compressions when turned on.

FDASep 14, 2006Nationwide• Michigan Instruments, Inc.

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 9000, 100v, with color screen; Mo...

The hand crank handle may separate and detach from the unit during use.

FDASep 14, 2006Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 8000 Base, 4 pump, 115v; Model 80...

The hand crank handle may separate and detach from the unit during use.

FDASep 14, 2006Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Manual Drive Unit for Sarns (Terumo) Centrifugal Perfusio...

The hand crank handle may separate and detach from the unit during use.

FDASep 14, 2006Nationwide• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 9000, 220/240v, with color screen...

The hand crank handle may separate and detach from the unit during use.

FDASep 14, 2006Nationwide• Terumo Cardiovascular Systems Corp

Medtronic Perfusion Systems: Medtronic Intersept Custom Tubing Pack. Do Not Reuse. T...

An out of specification condition exists with the tapered tubing found in some Custom Tubing Packs. The wall thickness is undersized and does not meet specifications.

FDASep 13, 2006CA, FL, IL +3 more• Medtronic Perfusion Systems