Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Neptune Plus Recalled by TZ Medical Inc. Due to The IFU of the Neptune Plus Pads, does...
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, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis following needle/sheath removal, Part number 8870-03
Quantity: 32,170 units
Why Was This Recalled?
The IFU of the Neptune Plus Pads, does not match that submitted in the original 510k. Need to remove: for haemostasis following needle/sheath removal
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About TZ Medical Inc.
TZ Medical Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report