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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 23061–23080 of 25000 recalls

Ventana Medical Systems Inc: Ventana Medical System's Symphony Staining System, KPA, M...

Shock hazard: Devices released prior to full testing; the configuration of the Symphony instrument during Hi pot testing procedures did not completely evaluate all components in the test loop. In specific circumstances, a shock hazard exists.

FDASep 6, 2007Nationwide• Ventana Medical Systems Inc

BD Diagnostic Systems Lee Laboratories: BD DifcoTM Neisseria Meningitidis Antisera Group Y, 2288...

Exhibits cross reactivity with Neisseria meningitides Group W135.

FDASep 6, 2007Nationwide• BD Diagnostic Systems Lee Laboratories

Medtronic Sofamor Danek USA Inc: Medtronic Sofamor Danek, Prestige Cervical Disc System, I...

Implant mis-seating; Variance in size between the trial and the implant could cause the implant to be improperly seated.

1...1152 115311541155 1156...1250

Page 1154 of 1250Next

FDA

Sep 4, 2007

Nationwide

• Medtronic Sofamor Danek USA Inc

Philips Medical Systems: HeartStart XL Defibrillator/Monitor, Model: M4735A

Inadequate shipping package causing damage to control boards resulting in unit failure. Failure to deliver therapy (defibrillation, pacing or cardioversion) may occur as a result of undetected damage to the PCB assembly.

FDASep 4, 2007PR• Philips Medical Systems

Warsaw Orthopedic, Inc. dba Medtronic SOFAMOR DANEK: Medtronic Sofamor Danek METRx (TM) System Bayonet Electro...

Packaging weakness may compromise sterility and instructions for use are inadequate.

FDASep 4, 2007Nationwide• Warsaw Orthopedic, Inc. dba Medtronic SOFAMOR DANEK

GE Healthcare Clinical Systems: GE LOGIQ 3 Expert ultrasound scanner with software versio...

Inaccurate guidelines: The BE9C is an optional, small radius Bi-planar convex probe intended for use with the LOGIQ 3 Expert system in Urology application. An attempt by the user to activate the biopsy guidelines while this probe is in use will cause incorrect guidelines to be displayed on the image. The incorrect guidelines are recognized by their orientation that is left/right reversed from t

FDASep 4, 2007AL, NY• GE Healthcare Clinical Systems

Toe-Space Electric Heaters (Berko Electric) – Fire Hazard (2007)

Fire/Burn Risk

The recall involves electric, toe-space heaters typically installed in kitchens and bathrooms at floor level in the recessed space under cabinets. The recall includes Berko Electric catalog numbers TS, TS-1 and TS-1A and Emerson Electric "Chromalox Comfort Heating" and "Environmental Products" catalog number KSH2000. The heater is controlled by a wall thermostat or a thermostat mounted on the front of the heater. The heater has a removable, black metal grille that measures 23 1/2 inches wide and 3 1/2 inches tall with five sets of openings, each with seven horizontal louvers.

CPSCAug 30, 2007Nationwide• Berko Electric, of Peru, Ind., now known as Marley Engineered Products, of Bennettsville, S.C.

Toshiba American Med Sys Inc: NEMIO XG Ultrasound System, Model SSA-580A , Software ver...

Multiple problems including : (1) The surface temperature of the transducer tip can rise and exceed the limit set by the international standard. (2) Incorrect display of the TI indices on the display monitor. The displayed value is greater or smaller than the true TI value, and (3) Manuals contain incorrect values for MI/TI values.

FDAAug 29, 2007Nationwide• Toshiba American Med Sys Inc

Toshiba American Med Sys Inc: NEMIO Ultrasound System, Model SSA-550A , Software versi...

FDAAug 29, 2007Nationwide• Toshiba American Med Sys Inc

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Paceart System, 2006 Edition, Medtronic, Inc. 7...

An issue with the Paceart System - 2006 First Edition (Get Connected Edition) exists. Under certain circumstances, Paceart System Generic ICD reports may not accurately reflect patient VT/VF, SVT/NST and Mode Switch/AT/AF episode detection data. When episode detection data is imported into the Paceart System from certain sources, the Paceart System Generic ICD reports display a zero, suggesting

FDAAug 27, 2007Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Sofamor Danek USA Inc: Medtronic Sofamor Danek, TSRH SiLo 5.5 Spinal System, Sag...

Disassembly: The movable cradle component could detach from the saddle under extreme manipulation of the associated rods prior to final tightening of the set screws.

FDAAug 24, 2007Nationwide• Medtronic Sofamor Danek USA Inc

Backpack Blowers (Shindaiwa) – Fire Risk (2007)

Fire/Burn Risk

This recall involves Shindaiwa Models EB8510 and EB8510RT. All models up to serial #7025018 are included. After serial number 7025018, the leaf blower has been upgraded with stainless steel muffler shells. The backpack blowers weight approximately 24 pounds and include Serial Numbers through February 2007 production (S/N 702XXXX) which are located on the side label. These machines are blue, with a red label that reads "Shindaiwa".

CPSCAug 24, 2007Nationwide• Shindaiwa Kogyo Co., Ltd., Hiroshima, Japan

Philips Medical Systems North America Co. Phillips: Philips Medical System - BV Pulsera Mobile C-arms with Re...

System Shut Down -- Unexpected Shut Down during use of the Optional Remote Control.

FDAAug 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Philips Medical System - Endura X-Ray Systems (Release 2)...

System Shut Down -- Unexpected Shut Down during use of the Optional Remote Control.

FDAAug 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Nuclear Medicine, Inc.: The Pinnacle3 Radiation Therapy Planning (RTP) system and...

Incorrect Absolute Marking Coordinates when used with PQ-Series scanners due to a software malfunction

FDAAug 21, 2007AL, AK, AZ +43 more• Philips Nuclear Medicine, Inc.

Ambu Incorporated: Ambu, Positive End Expiratory Pressure (PEEP) Valves, PEE...

Lower pressure than expected: Medical device for respiratory care may leak and not register accurate flow settings that affect patient respiration.

FDAAug 21, 2007Nationwide• Ambu Incorporated

Karl Storz Endoscopy America Inc 600 Corporate Pointe: Storz Equipment, Fluid Management Stand, for Fluid Manage...

Outflow Difference: The accuracy of the Equimat displayed value could be influenced by external factors of the cart/stand and may result in a fluctuating or inaccurate reading.

FDAAug 17, 2007Nationwide• Karl Storz Endoscopy America Inc 600 Corporate Pointe

Classic Beauty Rest Electric Throws – Safety Issue (2007)

Fire/Burn Risk

This recall involves 52 inch by 62 inch electric warming throws. The 100% acrylic throws were sold in various colors and patterns and have model number BST-06-THR. The model number is located on the care label sewn into the throw. "Classic Beautyrest" and "Automatic Electric Warming Throw" is printed on the product's packaging. Model numbers with the following date codes are included in this recall: B00106 through B36506. Bilt-Safe Technologies, Inc. and the date code are printed on the bottom of the care label.

CPSCAug 15, 2007Nationwide• Ningbo Veken Elite International Trading Company Ltd., of China

Merit Medical Systems, Inc: Merit Medical Surgical Convenience Kits, Custom and SPPT,...

Expiration Dating; Some Convenience Kits contain medications and/or skin preparations that may expire before the expiration date on the outer package label.

FDAAug 15, 2007Nationwide• Merit Medical Systems, Inc

Smiths Medical MD, Inc.: Smiths Medical CADD-Sentry Pro Medication Safety Software...

Incorrect dosage possible: A software anomaly in the CADD-Sentry Pro Administrator software (version B) where the values of a weight based protocol go to zero or round up to the next higher hundredths place, even if Administrator displayed the values correctly at data entry.

FDAAug 14, 2007CO, MD, UT• Smiths Medical MD, Inc.