FDA Enforcement Class II Terminated

TyTek Tension Pneumothorax Access Kit TPAK 14 gauge 3.25 inch- Intended for introduction into the body to facilitate removal of air from the pleural cavity in patients with a tension pneumothorax Model Number: TM-303

Recall: Z-2610-2023 · Reported September 27, 2023

Enforcement

Recall Number
Z-2610-2023
Event ID
92899
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Tytek Medical Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
September 27, 2023
Initiation Date
October 5, 2020
Classification Date
September 19, 2023
Termination Date
March 13, 2026
Address
8904 Beckett Rd, West Chester, OH, 45069-7054, United States

Description

TyTek Tension Pneumothorax Access Kit TPAK 14 gauge 3.25 inch- Intended for introduction into the body to facilitate removal of air from the pleural cavity in patients with a tension pneumothorax Model Number: TM-303

Reason

Updated IFU to inlclude: (1) identify the risks associated with the hazard of needle decompression and (2) improve the artwork showing placement site location

Code Info

UDI: 00855204008006 All lots produced prior to Oct 5, 2020

Distribution

OH, SC, VA Foreign: Country Australia Denmark Finland Germany Hong Kong/China Israel SPAIN The Netherlands Turkey UAE UK

Quantity

439146 units