FDAJuly 6, 2026
Pi-Cardia ShortCut Recall Over Positioning Arm Weld Issue
FDA published this notice on July 6, 2026 for United States.
This notice is kept at its address for anyone who saved the link. AreaZine no longer holds the agency's full record for it, so the page shows what AreaZine recorded and links to the agency's own page, the one to read.
What AreaZine recorded
- Agency
- FDA
- Place
- United States
- Date
- July 6, 2026
- Recall class
- Class II
- Reason given by the agency
- Transfemoral catheter, positing arm may detached due to weld issue.
- Distribution
- US Nationwide distribution in the states of Utah, Kansas, California, Massachusetts, Pennsylvania, New Hampshire, Delaware, and New York.
- Official source
- the notice at its source
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Source: FDA.