Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Pinnacle¿ Destination¿ Peripheral Guiding Sheath Recalled by Terumo Medical Corporation Due to Medical devices were incorrectly labeled with extended expiration...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Terumo Medical Corporation directly.
Affected Products
Pinnacle¿ Destination¿ Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve. Acts as a conduit to facilitate the introduction of interventional and diagnostic devices into the human vasculature.
Quantity: 20 units
Why Was This Recalled?
Medical devices were incorrectly labeled with extended expiration dates.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Terumo Medical Corporation
Terumo Medical Corporation has 18 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report