Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The suction valve may not close properly which...

Date: June 11, 2018
Company: Cardinal Health 200, LLC
Status: Terminated
Source: FDA (Device)

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 Cardinal Health 200, LLC directly.

Affected Products

Hydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Single Spike, Ref ASU1200, packaged 1/box, 12 boxes/case, single use, RX, Sterile.

Quantity: A total of 63,020 valves were distributed. Specific product quantities were not provided.

Why Was This Recalled?

The suction valve may not close properly which could cause continuous suction.

Where Was This Sold?

This product was distributed to 34 states: AL, AZ, AR, CA, CO, DE, FL, GA, IL, IN, IA, KS, KY, LA, MA, MI, MN, MO, MT, NV, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WY, DC

Affected (34 states)Not affected

About Cardinal Health 200, LLC

Cardinal Health 200, LLC has 275 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report