L-CATH PICC S/L Peripherally Inserted Central Catheter — Class II medical device recall Z-2638-2024
Ongoing recall by Argon Medical Devices, Inc, reported 2024-08-21, distributed in CA, IL, TX, WA. Peripherally Inserted Central Catheter (PICC) is labeled 26G/1.9Fr x 30cm but package contains incorrect 26G/1
| Recall number | Z-2638-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Argon Medical Devices, Inc, Athens, TX, United States |
| Recall initiated | 2024-06-14 |
| Classified | 2024-08-15 |
| Reported by FDA | 2024-08-21 |
| Distributed | CA, IL, TX, WA |
| Quantity | 155 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00886333209934, 20886333209938 |
| Lot numbers | 11563923 |
| Model numbers | 384539 |
| Expiration dates | 2027-03-11 |
Product
L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2638-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.