L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x 60c
FDA device recall Z-2803-2026 · posted 2026-07-24 · Open, Classified
Recall details
- Recalling firm
- Argon Medical Devices, Inc
- Reason for recall
- 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.
- Action taken
- On 6/15/2026, recall notices were emailed to customers who were asked to do the following: 1) Provide this recall notice to all people who need to be aware within your organization or to any organization where the potentially affected product has been transferred. 2) Segregate, quarantine, and return affected devices to recalling firm. 3) Complete and return the response form via email Arbee.cummings@argonmedical.com For additional information on this letter, please email Scott.Bishop@argonmedical.com
- Root cause
- Device Design
- Status
- Open, Classified
- Product code
- LJS
- Quantity affected
- 6928
- Distribution
- US: 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. OUS: MYS, CAN, SAU
- Date initiated
- 2026-06-15
- Date posted
- 2026-07-24
- Location
- Athens, TX
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters (K230669) | Argon Medical Devices | 2023-11-30 |