TZ Medical Recalls
4 recalls on record · June 5, 2013 to November 2, 2016 · Medical Devices
Recalls by year
13
15
16
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 2, 2016Medical DevicesFDA
TZ Medical, Inc. recalls Neptune Plus (Hemostatic Pad), Part Numbers: 8870-03 Neptune Pad is used to promote the rapid control of bleeding and p
Hazard: Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL BARRIER . This statement should not appear on label.
November 25, 2015Medical DevicesFDA
TZ Medical Inc. recalls SilverStat, sterile 2" x 2 " calcium alginate hemostasis pad with sliver nitrate, Part number 8870-07. Product
Hazard: During a review of the IFU of the SilverStat Pads, it was found that the IFU did not match that submitted in the original 510k
November 25, 2015Medical DevicesFDA
TZ Medical Inc. recalls Neptune Plus, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis following needle/sheath removal, Part number 887
Hazard: 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
June 5, 2013Medical DevicesFDA
TZ Medical Inc. recalls adult defibrillation, cardioversion, pacing, monitoring Disposable Electrodes, Model P-211-M1 and P-214-M1. Product U
Hazard: TZ 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