Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AMS 4675 Angio Pack. For use in a general clinical procedure. Recalled by Windstone Medical Packaging, Inc. Due to AMS 4675 Angio Pack is recalled because this...
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 Windstone Medical Packaging, Inc. directly.
Affected Products
AMS 4675 Angio Pack. For use in a general clinical procedure.
Quantity: 40 kits
Why Was This Recalled?
AMS 4675 Angio Pack is recalled because this kit containing U-SDN 2 Part Ultra Modified Seldinger Needle which is recalled by supplier.
Where Was This Sold?
This product was distributed to 2 states: AL, VA
About Windstone Medical Packaging, Inc.
Windstone Medical Packaging, Inc. has 315 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report