FDA DeviceClass IINotable
FDA Recall: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Description
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.
Hazard
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.
Remedy
20
Related Recalls
2026-08-05 · FDA_DEVICE
FDA Recall: L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga
Argon Medical Devices, Inc
2026-07-22 · FDA_DEVICE
FDA Recall: Arterial Line Kit 20ga x 6, REF: 400115A
Argon Medical Devices, Inc
2026-07-22 · FDA_DEVICE
FDA Recall: T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL
Argon Medical Devices, Inc
2026-07-22 · FDA_DEVICE
FDA Recall: General Biospy Tray, REF: GUTS1000
Argon Medical Devices, Inc