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MEDLINE INDUSTRIES, LP Northfield

MEDLINE INDUSTRIES, LP Northfield Recalls

All product recalls associated with MEDLINE INDUSTRIES, LP Northfield.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 1841–1860 of 37661 recalls

Wayson Hydrocolloid (Medline) – Sterility Compromise (2025)

There is a potential for the sterility of the device to be compromised.

Low

FDAFeb 19, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

Merge Cardio (Merge Healthcare) – Measurement Workflow Issue (2025)

When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

Moderate

FDAFeb 19, 2025Nationwide• Merge Healthcare, Inc.

Calais Grape Jelly (Elwood) – Undeclared Colors (2025)

Undeclared Allergen

Contains undeclared colors (FD&C Blue 1 and FD&C Red 40)

Class III

1...91 929394 95...1884

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Low

FDAFeb 19, 2025NJ, NY• Elwood International, Inc.

Revolution CT System (GE Medical) – Potential System Issue (2025)

GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.

Moderate

FDAFeb 18, 2025Nationwide• GE Medical Systems, LLC

Revolution CT ES System (GE Medical) – Potential System Issue (2025)

Moderate

FDAFeb 18, 2025Nationwide• GE Medical Systems, LLC

Revolution Apex CT System (GE Medical) – Potential System Issue (2025)

Moderate

FDAFeb 18, 2025Nationwide• GE Medical Systems, LLC

Avastin Intravitreal Injection (Turbare) – Sterility Concern (2025)

Lack of Assurance of Sterility: due to a quality control process deviation. During an internal quality assurance review, an Acceptable Quality Limit (AQL) inspection was not conducted on a statistically sound number of samples. This may result in the inability to assure that the impacted products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess and may lead to products of unacceptable quality.

Class IIModerate

FDAFeb 18, 2025Nationwide• Turbare Manufacturing