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411 PRESS
WarningRecall #Z-1778-2026Medical Device

Cook Incorporated Recalls COOK MEDICAL Arterial Pressure Monitoring Tray

Cook Incorporated · 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

COOK MEDICAL Arterial Pressure Monitoring Tray, Reference Part Number APMY-2.5-15-0-2.5 , Order Number G58412; Reference Part Number APMY-4.0-21J-1-12, Order Number G58419

Reason for Recall

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

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

Worldwide distribution.

Remedy

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

411 Press Analysis

A Class II FDA recall has been issued for a medical device from Cook Incorporated, initiated on March 5, 2026. Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. This recall covers 20 units, distributed internationally. While not the highest severity, consumers should exercise caution and stop using the product until the recall is resolved.

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