Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ARROW ENDURANCE" Extended Dwell Peripheral Catheter System Recalled by Arrow International Inc Due to Certain lots of peripheral catheter systems may be...
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 Arrow International Inc directly.
Affected Products
ARROW ENDURANCE" Extended Dwell Peripheral Catheter System, Catalog Numbers: EDC-00820 & EDC-00820-B
Quantity: 305
Why Was This Recalled?
Certain lots of peripheral catheter systems may be missing the safety latch, intended to minimize the risk of sharps injuries.
Where Was This Sold?
This product was distributed to 7 states: CO, FL, IL, NC, PA, SC, TX
About Arrow International Inc
Arrow International Inc has 431 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report