FDA recall record

Argon Medical Devices L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) recall — FDA Z-2638-2024

Peripherally Inserted Central Catheter (PICC) is labeled 26G/1.9Fr x 30cm but package contains incorrect 26G/1.9Fr x 50cm PICC, which could lead to…

Class IIclassification
Z-2638-2024official record ID
Aug 21, 2024report date

Recall record at a glance

Official recordZ-2638-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmArgon Medical Devices, Inc.
Report dateAug 21, 2024
Recall initiation dateJun 14, 2024
Quantity155
LocationAthens, TX, United States

Official product description

L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539

Why the product was recalled

Peripherally Inserted Central Catheter (PICC) is labeled 26G/1.9Fr x 30cm but package contains incorrect 26G/1.9Fr x 50cm PICC, which could lead to procedural delay.

Distribution information

US distribution to the states of: TX, WA, CA, IL

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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