Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to Cap-adapter assembly of the device may potentially not...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Cook Inc. directly.
Affected Products
Connecting Tube - Female to Male Luer Lock, HPCT8.8-60-M-FM Product Usage: The connecting tube is intended to be a conduit between a fluid reservoir and a vascular catheter in the patient. The connecting tube may be used during angiographic procedures to connect radiographic contrast power injector to a vascular catheter, arterial pressure monitoring, and fluid infusion.
Quantity: 220
Why Was This Recalled?
Cap-adapter assembly of the device may potentially not be adequately tightened, possibly leading to fluid leakage from or air aspiration into the connecting tube.
Where Was This Sold?
This product was distributed to 7 states: AL, CA, GA, NE, NV, NY, TX
About Cook Inc.
Cook Inc. has 262 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report