FDA recall record

Argon Medical Devices Scorpion Portal Vein Access Set - Product Usage: used to gain access recall — FDA Z-2501-2021

As a result of design changes, sheaths have exhibited cracking/breaking at the tips.

Class IIclassification
Z-2501-2021official record ID
Sep 29, 2021report date

Recall record at a glance

Official recordZ-2501-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmArgon Medical Devices, Inc.
Report dateSep 29, 2021
Recall initiation dateJul 8, 2021
Quantity20 units
LocationAthens, TX, United States

Official product description

Scorpion Portal Vein Access Set - Product Usage: used to gain access to the hepatic vein and guide a sharp puncture tool (0.040 Stylet or 17ga Needle) through the parenchyma.

Why the product was recalled

As a result of design changes, sheaths have exhibited cracking/breaking at the tips.

Distribution information

U.S. Nationwide distribution in the state of WA. O.U.S.: N/A

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.

About this record

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