Devices

Device Recall Tearaway Introducer

Model / Serial
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
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
US Distributed to: FL, TX, NC
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.
Manufacturer
Medical Components, Inc dba MedComp
1 Event
- Recall of Device Recall Tearaway Introducer

Manufacturer

Medical Components, Inc dba MedComp

Manufacturer Address
Medical Components, Inc dba MedComp, 1499 Delp Dr, Harleysville PA 19438-2936
Manufacturer Parent Company (2017)
Medical Components Inc.
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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