Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Tearaway Introducer Recalled by Medical Components, Inc dba MedComp Due to This recall has been initiated due to the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medical Components, Inc dba MedComp directly.
Affected Products
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.
Quantity: VS203 Lot# MBZX140 (100 units); VS303 Lot # MBZL450 (60 units); VS303 Lot # MBZV930 (65 units); VS303 Lot # MBZZ490 (33 units).
Why Was This Recalled?
This recall has been initiated due to the product labeled with the incorrect expiration date.
Where Was This Sold?
This product was distributed to 3 states: FL, NC, TX
About Medical Components, Inc dba MedComp
Medical Components, Inc dba MedComp has 38 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report