Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Neptune Plus (Hemostatic Pad) Recalled by TZ Medical, Inc. Due to Neptune Plus was mis-labeled and included the statement...
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 TZ Medical, Inc. directly.
Affected Products
Neptune Plus (Hemostatic Pad), Part Numbers: 8870-03 Neptune Pad is used to promote the rapid control of bleeding and provide hemostasis for lacerations, abrasions, vascular access sites and following surgical incision. It can be used to achieve hemostasis at the skin surface for arterial/venous catheterization/tubes, needle puncture, hemodialysis and in patients on anticoagulation therapy
Quantity: 1410 (141 boxes of 10)
Why Was This Recalled?
Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL BARRIER . This statement should not appear on label.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About TZ Medical, Inc.
TZ Medical, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report