TZ Medical, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0298-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 7, 2016

Date Posted: November 2, 2016

Recall Number: Z-0298-2017

Event ID: 74809

Reason for Recall:

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

Status: Terminated

Product Quantity: 1410 (141 boxes of 10)

Code Information:

Lot R970249

Distribution Pattern:

Nationwide Distribution to AL, CA, FL, GA, IL, IN, KY, MO, MS, NC, NV, NY, PA, SC, TN, TX, and WV.

Voluntary or Mandated:

Voluntary: Firm initiated