Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GALT Guidewire REF SGW-051-07 Guidewires are intended for use in Recalled by Galt Medical Corporation Due to Due to a potential open seal in the...
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 Galt Medical Corporation directly.
Affected Products
GALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedures, to introduce and position catheters and other interventional devices within the Coronary and peripheral vasculature.
Quantity: 100 guidewires
Why Was This Recalled?
Due to a potential open seal in the sterile barrier packaging.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Galt Medical Corporation
Galt Medical Corporation has 20 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report