Neptune Plus — Class II medical device recall Z-0298-2017
Terminated recall by TZ Medical, Inc., reported 2016-11-02, distributed nationwide. Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL BARRIER . This statement should no
| Recall number | Z-0298-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | TZ Medical, Inc., Portland, OR, United States |
| Recall initiated | 2016-07-07 |
| Classified | 2016-10-21 |
| Reported by FDA | 2016-11-02 |
| Terminated | 2016-10-28 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| Lot numbers | R970249 |
| Model numbers | 8870-03 |
Product
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
Reason for recall
Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL BARRIER . This statement should not appear on label.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0298-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.