FDA recall record

TZ Medical Neptune Plus, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis following recall — FDA Z-0293-2016

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

Class IIclassification
Z-0293-2016official record ID
Nov 25, 2015report date

Recall record at a glance

Official recordZ-0293-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTZ Medical Inc.
Report dateNov 25, 2015
Recall initiation dateOct 14, 2015
Quantity32,170 units
LocationPortland, OR, United States

Official product description

Neptune Plus, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis following needle/sheath removal, Part number 8870-03

Why the product was 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

Distribution information

US nationwide distribution.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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