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Medium risk Medical DevicesClass II

Medline Microdisectomy Pack Recall

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. MICRODISECTOMY PACK, Medline Kit Number/SKU DYNJ805

Updated March 19, 2026

Medline Microdisectomy Packs containing Neuro Sponges have higher-than-expected endotoxin levels, which can cause infection or inflammatory reactions during neurosurgery. Medline is voluntarily recalling affected kits.

Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on March 19, 2026. Details below.

What is recalled

Medline Microdisectomy Packs containing Medline Neuro Sponges, Kit Numbers: DYNJ80585B, DYNJ80585C, and DYNJ80585D.

Am I affected

You're affected if you are a healthcare facility with one of these Medline Microdisectomy Pack kit numbers in your inventory: DYNJ80585B, DYNJ80585C, or DYNJ80585D. Check your medical supplies for these SKU numbers.

What to do right now

Stop using these kits immediately. Contact Medline Industries directly for instructions on returning or replacing the affected Microdisectomy Packs (Kit Numbers DYNJ80585B, DYNJ80585C, DYNJ80585D).

The hazard

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

Brands affected

Medline Industries, LP
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-2030-2026
Classification
Class II
Recalled
March 19, 2026
Read the official notice

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