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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 2441–2460 of 37661 recalls

Sterile Kelly Hemostat (Medline) – Sterility Seal Weakness (2024)

Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.

Moderate

FDANov 12, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Reprocessed Bruns Curette (Medline) – Sterility Seal Weakness (2024)

Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.

Moderate

FDANov 12, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Bowl & Basket Onion Soup Mix – Undeclared Egg (2024)

Undeclared Egg

Undeclared egg

Class I

1...121 122123124 125...1884

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High

FDANov 12, 2024IN, NJ• Gilster-Mary Lee Corporation Cake Plant

IUD Removal Hook (Medline) – Sterility Seal Weakness (2024)

Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.

Moderate

FDANov 12, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Philips Allura Xper Systems (Philips) – Lifetime Extension Issue (2024)

Potential safety issues in Allura Xper R7.6- R8.1 systems where the Lifetime Extension (LTE) kit is not installed in a timely manner. Root cause is under investigation, but the recall reason is listed as for systems over 10 years of life with LTE kits are experiencing propeller motor clamping bolt and x-ray tube locking bolt breaks. If this happens, it may cause erratic C-arm movements and potential collision with patients or bystanders, or detection of a false collisions and subsequent blocked movement of the c-arm. Movement may also cause image noise and black area on the x-ray image, and possible need to expose the patient to additional unnecessary radiation during re-examination.

High

FDANov 11, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

TriALTIS Torque Limiter (Gauthier) – Torque Output Error (2024)

An out of specification component may result in the device exhibiting torque output higher than the design specification.

Moderate

FDANov 11, 2024Nationwide• Gauthier Biomedical, Inc.

2025 Forest River Impression (Forest River) – Electrical Line Defect (2024)

Fire/Burn Risk

Forest River, Inc. (Forest River) is recalling certain 2021-2025 Impression fifth wheel travel trailers. The solar charge line, front LED hitch light, and the pass-thru light may have been wired to the incorrect mini breaker.

High

NHTSANov 8, 2024Nationwide• FOREST RIVER

2024 Diamond C Pacesetter (Diamond C) – Axle Assembly Issue (2024)

Diamond C Trailer MFG (Diamond C) is recalling certain 2023-2024 MFG and Pacesetter trailers. Please see the recall report for a complete list of models. The weld between the axle frame bracket assembly and frame may fail, reducing the trailer's stability while being towed.

High

NHTSANov 8, 2024Nationwide• DIAMOND C TRAILERS

2025 Forest River V-RV (Forest River) – Air Conditioner Problem (2024)

Fire/Burn Risk

Forest River, Inc. (Forest River) is recalling certain 2024 Ahara, Entrada, 2022-2025 FR3, Georgetown, 2021-2023 Dynamax Isata, 2021-2025 Encore, Mirada, Pursuit, 2025 Sportscoach, V-Cruise, V-Sport, V-Tour, 2023 Sunseeker, and 2024-2025 V-RV motorhomes, equipped with General Electric air conditioners with a soft start device with part number ICM870-16A-BH5400. The air conditioner soft start device may fail and overheat.

High

NHTSANov 8, 2024Nationwide• FOREST RIVER

Access Intact PTH Assay (Beckman Coulter) – Sample Storage Issue (2024)

The reason for the recall is that EDTA and lithium heparin plasma samples that are stored in the DxI 9000 Access Immunoassay Analyzer sample wheel for a prolonged period before performing the intact PTH (parathyroid hormone) test may produce falsely decreased intact parathyroid hormone results. This could lead to a missed diagnosis, a delay in treatment, or inappropriate clinical management, depending upon the patient s clinical condition.

Moderate

FDANov 8, 2024Nationwide• Beckman Coulter Inc.

Levothyroxine Sodium Tablets (Accord Healthcare) – Subpotent Drug (2024)

Subpotent drug

Class IIModerate

FDANov 8, 2024Nationwide• ACCORD HEALTHCARE, INC.

Guaifenesin Dextromethorphan Syrup (Harvard Drug Group) – Specification Failure (2024)

Failed Impurity/Degradation Specifications

Class IIModerate

FDANov 7, 2024Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Major Neuro Pack Convenience Kit (Medline) – Endotoxin Level (2024)

Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods

Moderate

FDANov 6, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

2025 PJ Trailers LD (PJ Trailers) – Suspension Brake Issue (2024)

PJ Trailers is recalling certain 2024-2025 LD trailers. The air ride suspension brake axles may be installed incorrectly, resulting in reduced braking ability.

High

NHTSANov 6, 2024Nationwide• PJ TRAILERS