https://plainrecords.com/brand/tz-medical/New recalls of TZ Medical from FDA, CPSC and NHTSA records.en-ushttps://plainrecords.com/recall/device/z-0298-2017/https://plainrecords.com/recall/device/z-0298-2017/Wed, 02 Nov 2016 00:00:00 +0000Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL BARRIER . This statement should not appear on label.https://plainrecords.com/recall/device/z-0318-2016/https://plainrecords.com/recall/device/z-0318-2016/Wed, 25 Nov 2015 00:00:00 +0000During a review of the IFU of the SilverStat Pads, it was found that the IFU did not match that submitted in the original 510khttps://plainrecords.com/recall/device/z-0293-2016/https://plainrecords.com/recall/device/z-0293-2016/Wed, 25 Nov 2015 00:00:00 +0000The IFU of the Neptune Plus Pads, does not match that submitted in the original 510k. Need to remove: for haemostasis following needle/sheath removalhttps://plainrecords.com/recall/device/z-1438-2013/https://plainrecords.com/recall/device/z-1438-2013/Wed, 05 Jun 2013 00:00:00 +0000TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio Control Compatible transparent defibrillation electrodes because it may contain a defective white wire on the connector assembly. If a failure were to occur, the end user would be able to identify the failure by inspecting the white wire 1/4 inch from the Gray Medtronic / Physio adapter. The consignees will notice discolor