Recall Ledger

Medline medical convenience kit labeled as: TRACH TUBE KIT recall (Medline Industries, LP)

Medical deviceClass IIOngoing

Summary: Medline Industries, LP is recalling Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330. Reason: Component labeling discrepancy.

What is being recalled

Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330

Why

Component labeling discrepancy

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide distribution in the state of California. (states named: California)

How to tell if yours is affected

UDI/DI 10198459582158 (each) 40198459582159 (case), Lot Number 26FLA408

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-2999-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedJuly 10, 2026
ReportedSeptember 2, 2026
CompanyMedline Industries, LP
Company locationNorthfield, IL, United States
Initiated byVoluntary: Firm initiated
Quantity45 kits

More recalls from Medline Industries, LP · all medical device recalls · recalls from July 2026

Official FDA record