FDA · Medical devices ·
GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box recall
Terumo Medical Corporation recalled GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box on August 19, 2026 because of product was packaged with the 0.025 guidewire instead of the 0.021 guidewire. It was sold nationwide.
Why it was recalled
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
What's recalled
GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to facilitate placing a catheter through the skin into the radial artery.
Quantity: 7,490 units
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Terumo Medical Corporation, Elkton, MD
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
Worldwide distribution - US Nationwide and the country of Canada. - Status
- Ongoing
- Recall number
- Z-2930-2026
- Source
- U.S. Food and Drug Administration
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