FDA Medical Device Recalls (openFDA)
Argon Medical Devices, Inc: L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539
- Recall number
- Z-2638-2024
- Recalling firm
- Argon Medical Devices, Inc
- Product
- L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539
- Status
- Open, Classified
- Initiated
- 2024-06-14
- Posted
- 2024-08-16
- Terminated
- not on file
- Reason
- Peripherally Inserted Central Catheter (PICC) is labeled 26G/1.9Fr x 30cm but package contains incorrect 26G/1.9Fr x 50cm PICC, which could lead to procedural delay.
- Root cause
- Employee error
- Action
- On 6/14/24,"URGENT PRODUCT RECALL NOTICE"s were emailed to Physicians, Clinicians, or Hospital Administrators describing the product, problem and the following actions to be taken. The customers were instructed to do the following: 1) Immediately discontinue use of the recalled device. 2) Segregate and quarantine the product subject to recall. 3) Return all affected devices to firm at Argon s expense, using RGA# 28348 to the following mailing address: RGA# 28348, Argon Medical Devices, Inc.,1445 Flat Creek Road Athens, TX 75751 USA, Attn: Arbee Cummings. 4) The recall notice should be shared with anyone who needs to be aware within your organization or to any organization where the potentially affected products have been transferred or further distributed. 5) Complete and return the response form via email to arbee.cummings@argonmedical.com If you need assistance in returning the units, please contact arbee.cummings@argonmedical.com. If you have any questions about this letter, please contact Jorge.Garcia@argonmedical.com or Scott.Bishop@argonmedical.com.
- Quantity
- 155
- Distribution
- US distribution to the states of: TX, WA, CA, IL
- Lot, serial or model codes
- UDI-DI: 20886333209938, 00886333209934. Lot: 11563923. Expiration: 2027-03-11
- 510(k) numbers
- ["K230669"]
- PMA numbers
- not on file
- Product code
- LJS
- Firm FEI
- 1625425
- Firm city
- Athens
- Firm state
- TX
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28