Home / Recalls / Medical Devices
Medical Components, Inc dba MedComp recalls Tearaway Introducer, Model # VS203, VS303, 510 K # 130687, packaged individually in a pouch, 5 pouches per carton, lot #
Recalled June 15, 2016 · FDA recall Z-1924-2016 · Medical Components, Inc
Hazard
This recall has been initiated due to the product labeled with the incorrect expiration date. · FDA Class II
Units
VS203 Lot# MBZX140 (100 units); VS303 Lot # MBZL450 (60 units); VS303 Lot # MBZV930 (65 units); VS303 Lot # MBZZ490 (33 units).
Sold at
US Distributed to: FL, TX, NC
Description
This recall has been initiated due to the product labeled with the incorrect expiration date.
Product
Tearaway Introducer, Model # VS203, VS303, 510 K # 130687, packaged individually in a pouch, 5 pouches per carton, lot # MBZ140, MBZL450, MBZV930 MBZZ490 Product Usage: The 2F and 3F Vascu-Sheath Tearaway Introducer is intended for percutaneous venous access by modified Seldinger Technique in neonates, infants and children.
Manufacturer(s)
Medical Components, Inc dba MedComp
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →