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Tytek Medical Inc recalls TyTek PneumoDart- Intended for introduction into the body to facilitate removal of air from the pleural cavity in patien
Recalled September 27, 2023 · FDA recall Z-2612-2023 · Tytek Medical
Hazard
Updated IFU to inlclude: (1) identify the risks associated with the hazard of needle decompression and (2) improve the artwork showing placement site location · FDA Class II
Units
22,026 units
Sold at
OH, SC, VA Foreign: Country Australia Denmark Finland Germany Hong Kong/China Israel SPAIN The Netherlands Turkey UAE UK
Description
Updated IFU to inlclude: (1) identify the risks associated with the hazard of needle decompression and (2) improve the artwork showing placement site location
Product
TyTek PneumoDart- Intended for introduction into the body to facilitate removal of air from the pleural cavity in patients with a tension pneumothorax Model Number: TM-317
Manufacturer(s)
Tytek Medical Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →