Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm Recalled by Baxter Healthcare Corporation Due to Potential for the battery to lose its ability...
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 Baxter Healthcare Corporation directly.
Affected Products
FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm, 2.5 mm, 3.0 mm, 3.5 mm, 4.0 mm). Implantable device for vascular use.
Quantity: 109 units
Why Was This Recalled?
Potential for the battery to lose its ability to be recharged.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Baxter Healthcare Corporation
Baxter Healthcare Corporation has 401 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report