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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

398

Past Year

Class I (Serious)

Most Recent

Oct 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 21–40 of 398 recalls

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

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

FDAJul 1, 2024Nationwide• Neurovision Medical Products Inc

Titan Scaler Tip - Perio (Dental EZ Group) – Tip Seating Problem (2024)

Tip holder portion of the scaler tip assembly may have an oversized condition that will not allow the scaler tip to stay seated in the holder may cause injury

FDAMay 30, 2024Nationwide• Dental EZ Group Star Dental Division

Titan Blis-Sonic Scaler (Dental EZ Group) – Tip Seating Issue (2024)

Tip holder portion of the scaler tip assembly may have an oversized condition that will not allow the scaler tip to stay seated in the holder may cause injury

FDA

123 4...20

Page 2 of 20Next

May 30, 2024

Nationwide

• Dental EZ Group Star Dental Division

PROBEAT-FR (Hitachi) – Image Matching Software Error (2024)

During positioning within the system's 3D to 3D matching mode while transferring CBCT images, when the Float Image Selection button is pressed, it may display CBCT images that are insufficient in number.

FDAMay 27, 2024Nationwide• Hitachi America, Ltd., Particle Therapy Division

French's Crispy Fried Onions (McCormick) – Potential Bacterial Growth (2024)

Potential growth of Staphylococcus aureus

Class IIModerate

FDAMar 18, 2024AZ, IL• McCormick & Company, Inc.- Consumer Product Division

French's Crispy Fried Onions (McCormick) – Potential Bacterial Growth (2024)

Potential growth of Staphylococcus aureus

Class IIModerate

FDAMar 18, 2024AZ, IL• McCormick & Company, Inc.- Consumer Product Division

Angel Creme Chocolate Iced Donuts (Weis Markets) – Metal Contamination (2024)

Foreign material (metal) in donuts

Class IIModerate

FDAMar 15, 2024IN, PA• Weis Markets, Inc., Ice Cream Division

Angel Creme Powdered Donuts (Weis Markets) – Metal Contamination (2024)

Foreign material (metal) in donuts

Class IIModerate

FDAMar 15, 2024IN, PA• Weis Markets, Inc., Ice Cream Division

Peanut Butter Filled Iced Donuts (Weis Markets) – Metal Contamination (2024)

Foreign material (metal) in donuts

Class IIModerate

FDAMar 15, 2024IN, PA• Weis Markets, Inc., Ice Cream Division

Johnson & Johnson VISION Irrigation Sleeve (J&J) – Manufacturing Variation (2024)

Due to a manufacturing variation of the irrigation sleeves which could result in a missing port hole, this non-conformity could lead to insufficient flow to cool the ultrasonic phaco tip, potentially leading to an unstable anterior chamber which could cause possible harms.

FDAMar 14, 2024Nationwide• Johnson & Johnson Surgical Vision, Inc.

Trinias Angiography System (Shimadzu) – Flat Panel Malfunction (2024)

Due to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.

FDAJan 29, 2024Nationwide• SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Nishinokyo Kuwabara Cho Nakagyo-Ku

TactiFlex Ablation Catheter (St. Jude) – System Recognition Issue (2023)

When the catheters are used with the EnSiteX EP System, the system does not correctly recognize the catheter as the appropriate product model and instead reads and displays it as a different model. This results in some features specific to the catheter do not appear on the display and the catheter image may also appear inverted.

FDADec 18, 2023Nationwide• St. Jude Medical, Atrial Fibrillation Division, Inc.

TECNIS Toric II IOL (Johnson & Johnson) – Angle Specification Issue (2023)

Due to intraocular lens containing an angle out of specification (OOS). The cylinder axis marks do not meet product specifications for the allowable angle between Low Power Meridian (LPM) and toric cylinder axis marks.

FDADec 12, 2023Nationwide• Johnson & Johnson Surgical Vision, Inc.

AU/DxC Chemistry Transferrin (Beckman Coulter) – stability claims issue (2023)

The firm has identified that the Transferrin reagent does not meet the Instructions for Use (IFU) reagent on-board stability claims, which may cause control failures and/or erroneous patient samples results. The Complaint handling unit has received a total of 2 safety cases (CASE-2023-02027212 and CASE-2023-02045278) and 99 quality cases with the failure mode attributed to Transferrin reagent (OSR6152 / lot 2573) associated with reagent blank shifts for the Reagent 2 (R2), imprecision, calibration failures, erratic Quality Control (QC) recoveries, and/or erroneous high/low (serum, plasma, urine) patient results. The issue was confirmed through internal testing by Beckman Coulter on June 30, 2023. Reagent Blank shifts for R2, imprecision, calibration failures, erratic Quality Control (QC) recoveries, and/or erroneous high/low (serum, plasma, urine) patient results. The issue was confirmed through internal testing by Beckman Coulter on June 30, 2023.

FDASep 6, 2023Nationwide• Beckman Coulter Biomedical Division Lismeehan, O'Callaghan's Mills County Clare Ireland

Brownie Moose Tracks Ice Cream (Weis) – Undeclared Egg (2023)

Undeclared Egg

Undeclared egg

Class IHigh

FDAAug 30, 2023DE, IN, MD +5 more• Weis Markets, Inc., Ice Cream Division

ProCuity Bed Series (Stryker) – electrical safety test missing (2023)

Fire/Burn Risk

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

FDAAug 30, 2023Nationwide• Stryker Medical Division of Stryker Corporation

ProCurity Bed Series (Stryker) – electrical safety test missing (2023)

Fire/Burn Risk

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

FDAAug 30, 2023Nationwide• Stryker Medical Division of Stryker Corporation

TECNIS Eyhance IOL, REF: ICB00, STERILE.EO, Rx Only (Johnson & Johnson Surgical Vision, Inc.) – their is a potential that intraocular... (2023)

Their is a potential that intraocular lenses (IOLs) were manufactured with unintended toric fiducial marks.

FDAJul 6, 2023Nationwide• Johnson & Johnson Surgical Vision, Inc.

TECNIS Symfony, Extended Range of Vision IOL, REF: ZXR00,... (Johnson & Johnson Surgical Vision, Inc.) – their is a potential that intraocular... (2023)

Their is a potential that intraocular lenses (IOLs) were manufactured with unintended toric fiducial marks.

FDAJul 6, 2023Nationwide• Johnson & Johnson Surgical Vision, Inc.

Fargo Ortho-K Lens (PARAGON VISION SCIENCES, Inc) – manufactured lenses are not covered b... (2023)

Manufactured lenses are not covered by existing FDA approval

FDAJun 26, 2023Nationwide• PARAGON VISION SCIENCES, Inc