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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

278

Past Year

Class I (Serious)

Most Recent

Sep 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 41–60 of 278 recalls

Proxima Surgical Drape (Medline) – Packaging Sterility Risk (2025)

Potential breach in pouch packaging which could lead to loss of sterility.

Moderate

FDAFeb 13, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

Namic Convenience Kits (Medline) – luer fitting excess material (2025)

The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.

Moderate

FDAFeb 12, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

Medline C Section Pack (Medline) – syringe quality alert (2025)

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.

Moderate

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FDA

Feb 11, 2025

Nationwide

• MEDLINE INDUSTRIES, LP Northfield

ReNewal Livewire Catheter (Medline) – endotoxin levels (2025)

Devices may have higher than expected amounts of bacterial endotoxin.

Moderate

FDAFeb 6, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

Medline Convenience Kits (Medline) – Skin Barrier Issue (2025)

Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.

Moderate

FDAJan 9, 2025CA, NY• MEDLINE INDUSTRIES, LP Northfield

Medline RR-Liver Trans Kit (Medline) – Catheter Recall (2025)

Medline is recalling medical convenience kits which were assembled with specific Coloplast Foley catheters and Prostatic catheters which were subsequently recalled due to a potential sterility issue detected during testing.

Moderate

FDAJan 3, 2025CA• MEDLINE INDUSTRIES, LP Northfield

Medline Surgery Tray (Medline) – Catheter Hub Defect (2024)

The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.

Moderate

FDADec 31, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Centurion Infusion Catheter (Medline) – Mislabeling (2024)

Certain lots Sterile Infusion Catheters which were mislabeled as having a heparin coating were either distributed or manufactured into medical convenience kits and distributed.

Moderate

FDADec 23, 2024FL, IL, KS +4 more• MEDLINE INDUSTRIES, LP Northfield

Medline Arterial Line Pack (Medline) – Mislabeling (2024)

Certain lots Sterile Infusion Catheters which were mislabeled as having a heparin coating were either distributed or manufactured into medical convenience kits and distributed.

Moderate

FDADec 23, 2024FL, IL, KS +4 more• MEDLINE INDUSTRIES, LP Northfield

Medline Fluid Delivery Set (Medline) – Drip Chamber Mismatch (2024)

Fluid Delivery Sets were incorrectly assembled with a white macro drip chamber instead of the required grey micro drip chamber. The macro drip chamber delivers three times more fluid per drop than the micro drip chamber.

Moderate

FDADec 16, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

DocMan Kit (Medline) – Non-Sterile Components (2024)

Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.

Moderate

FDANov 21, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Medline Procedure Kits (Medline) – Non-Sterile Components (2024)

Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.

Moderate

FDANov 21, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Medline Procedure Kits (Medline) – Mask Quality Issue (2024)

Certain Medline kits were manufactured and distributed with Procedure Masks with SO SOFT Earloops, and SOFT TOUCH II Surgical Masks which were subsequently recalled for not meeting the bioburden testing requirements of EN 14683.

Moderate

FDANov 18, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Hudson RCI mBrace (Medline) – Adhesive and Pressure Issue (2024)

Complaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbones and upper lip which may cause dermal injury depending on the device positioning.

Moderate

FDANov 18, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield