FDA recall record

Argon Medical Devices PAC Tray/5 Catheter Introducer Tray 8F, Model 497424, Rx Only, STERILE recall — FDA Z-1938-2020

Arterial Line Kits include thicker curved reverse-cutting needle with a 0-silk suture, instead of the usual straight-cutting needle with a 3-0 silk…

Class IIclassification
Z-1938-2020official record ID
May 20, 2020report date

Recall record at a glance

Official recordZ-1938-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmArgon Medical Devices, Inc.
Report dateMay 20, 2020
Recall initiation dateApr 8, 2020
Quantity80
LocationAthens, TX, United States

Official product description

PAC Tray/5 Catheter Introducer Tray 8F, Model 497424, Rx Only, STERILE EO, UDI: 00886333214440 - Product Usage: The introducers are indicated for use in arterial and venous procedures requiring percutaneous introduction of intravascular devices. Curved tip Introducer allows for contralateral access to the iliac artery and selected vasculature. Case Label: PAC Tray/5 Catheter Introducer Tray 8F, QTY 10/Bx, Rx Only, STERILE EO

Why the product was recalled

Arterial Line Kits include thicker curved reverse-cutting needle with a 0-silk suture, instead of the usual straight-cutting needle with a 3-0 silk suture. The thicker suture may be more difficult to tie. The curved needle requires the use of a needle driver, there is a risk of needle stick to the surgeon tries to do it with fingers instead.

Distribution information

US Nationwide distribution including the states of CA, IL, ND, SC, TX, VA. OUS: None

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

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