Medical device recalls Moderate risk

Medline Industries, LP recalls MEDLINE ANTERIOR HIP PACK DYNJ64672B

Recall date
February 16, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1711-2026
FDA classification
Class II
Brand / firm
Medline Industries, LP
Sold / distributed
US Nationwide distribution in the states of CA, FL, IL, IN, KY, MA, MD, MT, NY, OH, PA, TN, TX.

Why it was recalled

Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

MEDLINE ANTERIOR HIP PACK DYNJ64672B

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