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
2013–20261314151617181920212223242526
Class I (FDA, most serious)Other recalls
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…
No recalls match.
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.