Medical Device Recall: 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 va
Galt Medical Corporation · March 27, 2025
Reason for Recall
Due to a potential open seal in the sterile barrier packaging.
Product Description
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.
Distribution
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.
States Affected
NATIONWIDE
Quantity Affected
100 guidewires
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1734-2025
Status: ongoing
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