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Galt Medical Corporation recalls GALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedures, to introduce and position
Recalled May 14, 2025 · FDA recall Z-1734-2025 · Galt Medical
Hazard
Due to a potential open seal in the sterile barrier packaging. · FDA Class II
Units
100 guidewires
Sold at
Worldwide - U.S. Nationwide distribution in the states of AL, FL, GA, IL, MA, OH, PA, and UT. The countries of Canada, Ireland, Israel, Korea, Qatar, and United Kingdom.
Description
Due to a potential open seal in the sterile barrier packaging.
Product
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.
Manufacturer(s)
Galt Medical Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →