FDA Device recall Z-2804-2026
L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
- FDA Device
- Class II
- ongoing
- Published 2026-08-05
On 2026-08-05 the FDA classified a Class II recall of L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620 by Argon Medical Devices, citing catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2804-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-06-15 |
| Published | 2026-08-05 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Argon Medical Devices |
| Distribution | AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OR, TN, TX, UT, VA, WA |
Product
L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Reason
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.
Identifiers
| code_info | REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2804-2026%22
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