Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SurFlo IV Catheter Recalled by Terumo Medical Corporation Due to According to the Terumo (TMC) this device is...
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
SurFlo IV Catheter
Quantity: 2,478,200
Why Was This Recalled?
According to the Terumo (TMC) this device is used to access the human peripheral vascular system for short term use (less than 30 days) for the purpose of infusing fluids into patients. A small percentage of the catheters in the affected lots may have damage to the ETFE catheter which may allow the catheter to break during withdrawal.
Where Was This Sold?
US Distribution. This product has been sold to both distribution companies with multiple locations and directly to end users/hospitals in US.
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