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
FDA Recall Z-1938-2020 · Posted None
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Recalling FirmArgon Medical Devices, Inc
Recall StatusTerminated
Product CodeGDY
Date Initiated2020-04-08
Date Terminated2022-12-14
Product Quantity80
Reason for Recall
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.
Firm Action
Argon Medical Devices, Inc. sent Urgent Medical Device Recall letters, dated April 7, 2020 by mail on April 8th to the affected customer/hospital/distributors. The letter states they shipped Arterial Line Kits that include a different suture set than what is normally packaged in the kits the customers order. The kits customers normally order include a straight-cutting needle with a 3-0 silk suture. The kits customers recently received from them include a curved reverse-cutting needle with a 0-silk suture.
A list of the affected product numbers is provided in the letter. They immediately corrected the production error that created this situation and reestablished their supply of Arterial Line Kits with the correct suture set. If customers would like to exchange the Arterial Line Kits they
received for kits containing the correct suture set, they will gladly exchange these kits at no cost.
Conversely, they understand the rise of the recent COVID-19 pandemic put Arterial Line Kits in high demand in the United States. Therefore, they do not require customers to return the affected Arterial Line Kits if
they would prefer to use them as-is.
To facilitate an exchange of the product received customers can contact Argon Medical Customer Service at 1-800-927-4669 or [email protected]. If customers would prefer to use the product as-is, no further action is necessary.
The letter included a form for customers to acknowledge receipt and account for product inventory and submit for exchange if they wish.
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution including the states of CA, IL, ND, SC, TX, VA. OUS: None
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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