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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

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 23421–23440 of 25000 recalls

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

Iris Sample Processing: StatSpin Express 3 Centrifuge with RTX8 Rotor Model: M502

Rotor may crack and separate causing device to fail. A failed rotor not successfully contained may seriously injure the laboratory worker.

FDASep 29, 2006Nationwide• Iris Sample Processing

Eatonform Inc: Doc-U-Dose Prescription Management System, Item 8-PKIT. ...

The poly film may separate along the sealed seams of the packets of the Doc-U-Dose Prescription Management System causing the medications to unintentionally fall out of the packets prior to delivery to patient/consumers.

1...1170 117111721173 1174...1250

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FDASep 28, 2006Nationwide• Eatonform 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.

Suave Kids Bath Set (Almar) – Choking Risk (2006)

Choking Hazard

This recall involves "Suave" brand bath sets that contain a 2-in-1 shampoo, bath sponge, and various other toy animal and character bath products. The baths sets are packaged in brightly colored vinyl bags with a clear window. Style numbers involved in this recall are: SVK 9498, 9499, 9501, 9506, 9507 and 9508. The style numbers are located on the back and/or bottom right corner of the package, above the UPC code.

CPSCSep 27, 2006Nationwide• Almar Sales Co., of New York, NY

Belcher Pharmaceuticals Inc.: Product is Mucotrol Concentrated Oral Gel Wafer contained...

Processing and cleaning process validation were not completed before production. Product had some GMP failures related to the quality system.

FDASep 25, 2006Nationwide• Belcher Pharmaceuticals 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

USA Instruments Incorporated: 3.0T HD Head Neck Spine Array, Model 2415545, for GE 3....

Fire/Burn Risk

The firm determined that certain potential conditions for use of their medical device, outside of recommended practices, or operating manual descriptions, could result in a localized RF burn and/or electrical shock to a patient on which the device is being used.

FDASep 20, 2006CA, FL, IA +6 more• USA Instruments Incorporated

USA Instruments Incorporated: 1.5T HD Head Neck Spine Array, Model 2416329, for GE 1.5T...

Fire/Burn Risk

FDASep 20, 2006CA, FL, IA +6 more• USA Instruments Incorporated

Arctic Cat Snowmobile – Steering Failure (2006)

Fire/Burn Risk

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.

Datex Ohmeda, Inc: Datex-Ohmeda Tec 6 Plus Desflurane Vaporizer. It is an e...

There is a possibility of a vaporizer power failure, with audible and visual alarms, when using the Tec 6 Plus Desflurane Vaporizer.

FDASep 15, 2006Nationwide• Datex Ohmeda, Inc

Advanced Medical Optics, Inc.: COMPLETE Multi-Purpose Solution (Asia Pacific markets, ex...

Due to a potential sterility issue with the product container. Three lots sold in Japan were found to have bacterial contamination, which compromised sterility. Because of this production-line issue at the firm''s plant in China, AMO is recalling lots that were manufactured on the same production lines during the same production period.

FDASep 15, 2006Nationwide• Advanced Medical Optics, Inc.

Advanced Medical Optics, Inc.: COMPLETE MoisturePLUS Multi-Purpose Solution (US and As...

Due to a potential sterility issue with the product container. Three lots sold in Japan were found to have bacterial contamination, which compromised sterility. Because of this production-line issue at the firm's plant in China, AMO is recalling lots that were manufactured on the same production lines during the same production period.

FDASep 15, 2006Nationwide• Advanced Medical Optics, Inc.

Advanced Medical Optics, Inc.: Krystal Klear Rinse (China only)

Due to a potential sterility issue with the product container. Three lots sold in Japan were found to have bacterial contamination, which compromised sterility. Because of this production-line issue at the firm's plant in China, AMO is recalling lots that were manufactured on the same production lines during the same production period.

FDASep 15, 2006Nationwide• Advanced Medical Optics, Inc.

Advanced Medical Optics, Inc.: Lens Plus Ocupure Saline Sterile Rinsing Solution (Asia P...

FDASep 15, 2006Nationwide• Advanced Medical Optics, 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.

Class IHigh

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

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

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