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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

283

Past Year

Class I (Serious)

Most Recent

Jul 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 283 recalls

ReNewal Coblator II ENT Evac Wand (Medline) – Drip Chamber Disconnection (2025)

Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.

FDAMar 5, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

ReNewal ENT Coblator II PROcise Wand (Medline) – Drip Chamber Disconnection (2025)

Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.

FDAMar 5, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

ReNewal Coblator II Plasma Wand (Medline) – Drip Chamber Disconnection (2025)

Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.

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Page 2 of 15Next

FDA

Mar 5, 2025

Nationwide

• MEDLINE INDUSTRIES, LP Northfield

Medline Kits (Medline) – Packaging Seal Weakness (2025)

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

FDAMar 3, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

Medline Convenience Kits (Medline) – Packaging Seal Weakness (2025)

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

FDAMar 3, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

Medline Convenience Kits (Medline) – Tube Recall Issue (2025)

Specific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently recalled by Smiths Medical.

FDAFeb 24, 2025CA• MEDLINE INDUSTRIES, LP Northfield

Medline Procedure Kits (Medline) – Cannula Concern (2025)

Medline medical procedure kits, containing Medtronic Aortic Root Cannula

FDAFeb 21, 2025CA, FL, MN +6 more• MEDLINE INDUSTRIES, LP Northfield

Medline Procedure Kits (Medline) – Male Luer Material Issue (2025)

Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.

FDAFeb 21, 2025CA, FL, MN +6 more• MEDLINE INDUSTRIES, LP Northfield