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Brand recall history

TZ Medical recalls

Every FDA recall record we found for TZ Medical, newest first. Updated Oct. 11, 2026.

4

4 recalls since 2013. The most recent was on Nov. 2, 2016.

Last 12 months
0
Most recent
2016-11
Most serious (FDA Class I)
0
Last 30 days
0

Recalls by year

2013–2026
1
2
1
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Class I (FDA, most serious)Other recalls

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All recalls

4
  • Nov. 2, 2016Neptune Plus (Hemostatic Pad)… Class IINeptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL BARRIER . This statement should not appear on label.
  • Nov. 25, 2015SilverStat… Class IIDuring a review of the IFU of the SilverStat Pads, it was found that the IFU did not match that submitted in the original 510k
  • Nov. 25, 2015Neptune Plus… Class IIThe IFU of the Neptune Plus Pads, does not match that submitted in the original 510k. Need to remove: for haemostasis following needle/sheath removal
  • June 5, 2013adult defibrillation… Class IITZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio Control Compatible transparent defibrillation electrodes because it may…

How we match: a recall is listed here when the agency names TZ Medical as the company that filed it. Sources: FDA enforcement reports and FDA-posted company announcements, CPSC recall notices and NHTSA recall campaigns.

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