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Neurovision Medical Products Inc

Neurovision Medical Products Inc Recalls

All product recalls associated with Neurovision Medical Products Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

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 2021–2040 of 21320 recalls

Cobra 3-Plate EMG ET Tube (Neurovision) – Incorrect Tube Size (2024)

mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.

Low

FDAJul 1, 2024Nationwide• Neurovision Medical Products Inc

Everest Bipolar Cutting Forceps (Olympus) – Packaging Breach (2024)

Fractures and breakages in packaging trays and Tyvek covers, which may result in a sterility breach

High

FDAJul 1, 2024Nationwide• Olympus Corporation of the Americas

Fludrocortisone Acetate Tablets (Teva) – Impurity Concerns (2024)

Failed Impurities/Degradation Specifications: Product is being recalled due to API related substances and unknown impurities that are above the specification limits.

Class IIModerate

1...100 101102103 104...1066

Page 102 of 1066Next

FDA

Jun 28, 2024

Nationwide

• Teva Pharmaceuticals USA, Inc

Pravastatin Sodium Tablets (Glenmark) – Dissolution Failure (2024)

Failed Dissolution Specifications: results below specifications

Class IIModerate

FDAJun 28, 2024Nationwide• Glenmark Pharmaceuticals Inc., USA

IntelliVue Patient Monitor MX400 (Philips) – Software Configuration (2024)

Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded with Incorrect Software Options. Changes were made to reflect some options becoming standard capabilities for software-version N.x. In the process, the entitlements of software options MOS, M06, and M20 were removed for software versions L.x and M.x. As a result of these changes Patient Monitors manufactured with or updated to the latest versions of software L.x or M.x will not offer the capabilities> Mmonitors with software version K.x may experience this issue too, due to software version K being out of support and the devices being provided with L.x entitlements offered by software options MOS, M06, and M20. Potential for incorrect or delayed treatment for the patient,

Low

FDAJun 28, 2024Nationwide• Philips North America Llc

IntelliVue Patient Monitor MX500 (Philips) – Software Configuration (2024)

Low

FDAJun 28, 2024Nationwide• Philips North America Llc

2023 Micro Bird MB II School Bus (Micro Bird) – Door Handle Issue (2024)

Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2008-2025 G5, 2008-2024 MBII, and 2015-2024 T-Series school buses. The rear emergency door exterior handle may unexpectedly break under applied force.

High

NHTSAJun 27, 2024Nationwide• MICRO BIRD

Cyanocobalamin Injection (Zydus) – Glass Particulate Risk (2024)

Presence of particulate matter: glass

Class IIModerate

FDAJun 27, 2024TN• Zydus Pharmaceuticals (USA) Inc

2020 Micro Bird T-Series Transit Bus (Micro Bird) – Door Handle Problem (2024)

Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2008-2024 G5, 2008-2015 MBII, and 2015-2023 T-Series transit buses. The rear emergency door exterior handle may unexpectedly break under applied force.

High

NHTSAJun 27, 2024Nationwide• MICRO BIRD

Ventana Anti-CD10 Antibody (Ventana) – Staining Inaccuracy (2024)

Their is a potential for high background and off-target staining when using the monoclonal primary antibody which can result in false positive results.

Low

FDAJun 27, 2024Nationwide• Ventana Medical Systems, Inc.

Capio SLIM Suture Device (Boston Scientific) – Capture Inconsistency (2024)

Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.

Moderate

FDAJun 27, 2024Nationwide• Boston Scientific Corporation

CADD Medication Cassette Reservoir (Smiths Medical) – Weld Joint Weakness (2024)

Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.

Moderate

FDAJun 26, 2024Nationwide• Smiths Medical ASD Inc.

DVOT SARS-CoV-2 Antigen Test (Feng Chun Yuan) – Unauthorized Sales (2024)

The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.

Low

FDAJun 26, 2024Nationwide• FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN) CO., LTD No. 1304 Science And Technology Innovation Park, Shajing Dahong Shenzhen China

CADD-Solis Battery Pack (Smiths Medical) – Adapter Damage Risk (2024)

The adapter input plug can become damaged or broken. If the input plug is damaged, the metal contacts to the body of the AC adapter may be exposed or one or more of the AC mains prongs may separate from the input plug.

High

FDAJun 26, 2024Nationwide• Smiths Medical ASD, Inc.

DVOT Multi-Pathogen Antigen Test (Feng Chun Yuan) – Unauthorized Sales (2024)

The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.

Low

FDAJun 26, 2024Nationwide• FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN) CO., LTD No. 1304 Science And Technology Innovation Park, Shajing Dahong Shenzhen China

ENT Reservoir Kit (Smiths Medical) – Weld Joint Weakness (2024)

Moderate

FDAJun 26, 2024Nationwide• Smiths Medical ASD Inc.

BD Insyte Autoguard IV Catheter (BD) – Tubing Hole Risk (2024)

Catheters may contain a hole in the catheter tubing, which could result in leakage during the insertion process.

Low

FDAJun 26, 2024IL• Becton Dickinson Infusion Therapy Systems, Inc.

DVOT SARS-CoV-2 Antigen Test (Feng Chun Yuan) – Unauthorized Sales (2024)

The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.

Low

FDAJun 26, 2024Nationwide• FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN) CO., LTD No. 1304 Science And Technology Innovation Park, Shajing Dahong Shenzhen China

Sea Electric Battery Management System (Sea Electric) – Software Problem (2024)

SEA Electric LLC (SEA Electric) is recalling certain battery management system (BMS) software for electric vehicles. The BMS software can cause the high-voltage battery to shut down, resulting in a loss of drive power.

High

NHTSAJun 25, 2024Nationwide• SEA ELECTRIC

Potassium Chloride Capsules (Amerisource) – Dissolution Failure (2024)

Failed Dissolution Specifications

Class IHigh

FDAJun 25, 2024Nationwide• Amerisource Health Services LLC