Reported Nov 2, 2016 · Terminated

Neptune Plus (Hemostatic Pad), Part Numbers: 8870-03 Neptune Pad is used to promote the rapid control of bleeding and…

TZ Medical, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: TZ Medical, Inc. · 17750 SW Upper Boones Ferry Rd Ste 150 · Portland, OR · 97224-7086

Is this the product you have?

  • Neptune Plus (Hemostatic Pad)
  • Part Numbers8870-03 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
Lot codes and dates
  • Lot R970249
Amount recalled
1410 (141 boxes of 10)

Where it was sold

Why it was recalled

Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL BARRIER. This statement should not appear on label.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 28, 2016 · Data as of Sep 19, 6:49 PM UTC

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