No image published for this recall

L-Cath PICC S L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x 60cm, REF: 384464

Official notice

5 Aug 2026

Last checked

22 Sept 2026

MediumFDA

An official FDA notice concerns Argon Medical Devices. The notice reports an infection risk. Stop using the product and follow the official notice. Published 2026-08-05. Recall numbers: Z-2803-2026. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

6,928

Recall number

Z-2803-2026

Official notice

2026-06-15

The hazard

Infection risk

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Event Ids

99333

Recall Numbers

Z-2803-2026

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Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States · AR

Location 2

US · United States · CA

Location 3

US · United States · CO

Location 4

US · United States · CT

Location 5

US · United States · FL

Location 6

US · United States · GA

Location 7

US · United States · IA

Location 8

US · United States · ID

Location 9

US · United States · IL

Location 10

US · United States · IN

Location 11

US · United States · KS

Location 12

US · United States · MA

Location 13

US · United States · MD

Location 14

US · United States · MI

Location 15

US · United States · MN

Location 16

US · United States · MO

Location 17

US · United States · MS

Location 18

US · United States · NC

Location 19

US · United States · ND

Location 20

US · United States · NJ

Location 21

US · United States · NV

Location 22

US · United States · NY

Location 23

US · United States · OR

Location 24

US · United States · TN

Location 25

US · United States · TX

Location 26

US · United States · UT

Location 27

US · United States · VA

Location 28

US · United States · WA

Affected area 1

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Argon Medical Devices. Contact: Argon Medical Devices, Inc.

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class II

App estimate

medium

Recall details

Recall number

Z-2803-2026

Event id

99333

Units affected

6,928

Status

active

Classification

Class II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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