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FDA · Medical devices ·

Medline convenience kits labeled as recall

Medline Industries, LP recalled Medline convenience kits labeled as on September 2, 2026 because of kits contain a potentially contaminated component which were recalled by the manufacturer. It was sold nationwide.

Why it was recalled

Kits contain a potentially contaminated component which were recalled by the manufacturer

What's recalled

Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104; 3) CRANIOTOMY, Medline Kit SKU DYNJ903471I; 4) KIT CRANIOTOMY RFD, Medline Kit SKU DYNJ906496K.

Quantity: 241 kits

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Medline Industries, LP, Northfield, IL
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
US Nationwide distribution in the states of AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, WI.
Status
Ongoing
Recall number
Z-3029-2026
Source
U.S. Food and Drug Administration

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