Reported Aug 5, 2026 · Ongoing
L-Cath PICC S/L Peripherally Inserted Central Catheter
Argon Medical Devices, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Argon Medical Devices, Inc · 1445 Flat Creek Rd · Athens, TX · 75751-5002
Is this the product you have?
L-Cath PICC S/L Peripherally Inserted Central Catheter
4 products · 19 lot codes
38453918ga (3.5F) 1.15mm x 60cm
- UDI-DI
00886333209934
7 recalled lot codes
114881677/14/2026114881687/17/202611494535E8/1/20261150776611/13/20261155078012/12/20261155148712/15/20261155148812/15/2026
384464Basic Kit 28GA (1.2F) x 25cm 1 Lumen)
- UDI-DI
00886333209835
2 recalled lot codes
114905937/28/202611494886(8/28/2026)1150115010/6/2026
38451620ga (3F) 1.00mm x 60cm
- UDI-DI
00886333209910
8 recalled lot codes
115004108/14/2026115018568/14/2026115042229/9/2026115069529/9/2026115238689/18/2026115517899/18/20261155390911/13/20261155922611/20/2026
384463
- UDI-DI
00886333209828
2 recalled lot codes
114907978/1/2026114909598/11/2026
- Amount recalled
- 6928
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/aspirate catheter, catheter occlusion, therapy interruption, blood loss, tissue irritation, bloodstream infection.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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