Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Transonic ADT1018 Flow QC Clear Advantage Tubing Recalled by Transonic Systems Inc Due to The sterility of the device cannot be assured....
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 Transonic Systems Inc directly.
Affected Products
Transonic ADT1018 Flow QC Clear Advantage Tubing, Catalog No. ADT1018, ADT1018-40 The device is indicated for use as part of an extracorporeal blood circuit for hemodialysis when a monitor will be used to make access flow, recirculation, and/or cardiac output measurements during the patient s hemodialysis treatment.
Quantity: 6044
Why Was This Recalled?
The sterility of the device cannot be assured. There is a potential for an increased risk of infection.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Transonic Systems Inc
Transonic Systems Inc has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report