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WarningRecall #Z-1846-2026Medical Device

Medline Industries Recalls Medline Kits: 1) GYN LAPAROSCOPY PACK

Medline Industries, LP · Class II — Moderate Risk

Hospital operating room medical equipment — representative photo for FDA medical device recall
A hospital operating room with medical equipment (representative file photo). Specific recalled device: see recall details below. Photo: FDA / Public Domain.

Product Description

Medline Kits: 1) GYN LAPAROSCOPY PACK, Model Number: DYNJ41257F

Reason for Recall

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

FDA Classification

Class II — Moderate Risk

A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

Distribution

US Nationwide distribution.

Remedy

Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.

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