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FDA · Medical devices ·

Medline medical convenience kits labeled as recall

Medline Industries, LP recalled Medline medical convenience kits labeled as on July 29, 2026 because of medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species. It was sold in CT, FL, KS, OH, OR, NY, MD, MT, VA, MA.

Why it was recalled

Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.

What's recalled

Medline medical convenience kits labeled as: 1) TOTAL JOINT PACK Medline Kit SKU DYNJ65065A: 2) EXTREMITY/FOOT PACK Medline Kit SKU DYNJ65066B: 3) ANTERIOR CERVICAL-SMH Medline Kit SKU DYNJ907718B: 4) LAMINECTOMY-SMH Medline Kit SKU DYNJ907732C: 5) KYPHOPLASTY Medline Kit SKU DYNJ907984C: 6) LUMBAR LAMINECTOMY Medline Kit SKU DYNJ907987D: 7) KYPHOPLASTY TRAY Medline Kit SKU DYNJ908413C: 8) CRANIOTOMY Medline Kit SKU DYNJ910626: 9) NEURO SPINE Medline Kit SKU DYNJ910639.

Quantity: 1601 units

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
CT, FL, KS, OH, OR, NY, MD, MT, VA, MA
US: CT, FL, KS, OH, OR, NY, MD, MT, VA, MA.
Status
Ongoing
Recall number
Z-2791-2026
Source
U.S. Food and Drug Administration

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