Terumo Medical Corporation: Introducer, Catheter
Recall Summary Terumo Medical Corporation is recalling Glidesheath Slender A-Kit 6F 10CM catheters (Product Code 60-1060) because some units were packaged with an incorrect 0.025 guidewire instead of the correct 0.021 guidewire. This device is used to place catheters into the radial artery. The affected product was distributed nationwide in the US and Canada.
- Recalling firm
- Terumo Medical Corporation
- Product
- 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.
- Reason
- Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-06-15
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Worldwide distribution - US Nationwide and the country of Canada.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/4d3553be-c3ce-4f75-9a2d-32a77e24b366