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Medium risk Electronics & LightingClass II

Medline Industries, LP Recall

Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104;

Updated July 10, 2026

Medline Industries, LP is recalling Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104;. Hazard: Kits contain a potentially contaminated component which were recalled by the manufacturer

Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on July 10, 2026. Details below.

What is 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.

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

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

Brands affected

Medline Industries, LP
Source
FDA
Category
Electronics & Lighting
Recall ID
fda-Z-3029-2026
Classification
Class II
Recalled
July 10, 2026
Read the official notice

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