Medical Components, Inc dba MedComp: Medical Device Recall in 2016 - (Recall #: Z-1924-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: May 5, 2016

Date Posted: June 15, 2016

Recall Number: Z-1924-2016

Event ID: 74176

Reason for Recall:

This recall has been initiated due to the product labeled with the incorrect expiration date.

Status: Terminated

Product Quantity: VS203 Lot# MBZX140 (100 units); VS303 Lot # MBZL450 (60 units); VS303 Lot # MBZV930 (65 units); VS303 Lot # MBZZ490 (33 units).

Code Information:

Catalog Numbers/Lot Numbers/Exp. Date/UDI Number: VS203 Lot # MBZX140 exp. date 01/18/2021 UDI# 884908105209 VS303 Lot # MBZL450 exp. date 11/14/2020 UDI# 884908105216 VS303 Lot # MBZV930 exp. date 11/01/2021 UDI# 884908105216 VS303 Lot # MBZZ490 exp. date 01/28/2021 UDI# 884908105216

Distribution Pattern:

US Distributed to: FL, TX, NC

Voluntary or Mandated:

Voluntary: Firm initiated