Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arrow Glide Thru Peel-Away Sheath/Dilator Introducer Recalled by Arrow International Inc Due to Arrow is recalling additional lots that were identified...
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 Glide Thru Peel-Away Sheath/Dilator Introducer
Quantity: 9,037 units in the U.S. and 4,505 Internationally
Why Was This Recalled?
Arrow is recalling additional lots that were identified as part of an active recall. Arrow is recalling the affected product due to the possibility that the catheter peel-away component hub tabs may prematurely detach when the practitioner begins to peel apart the sheath body from the catheter.
Where Was This Sold?
This product was distributed to 11 states: AL, AZ, CA, GA, IN, MA, NJ, PA, SC, VA, WA
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