UltraStream Chronic Hemodialysis Catheter Standard Kit — Class II medical device recall Z-2696-2014
Terminated recall by Argon Medical Devices, Inc, reported 2014-10-01, distributed nationwide. UltraStream Chronic Hemodialysis Catheter may develop cracks on the red (arterial) luer during attachment or m
| Recall number | Z-2696-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Argon Medical Devices, Inc, Athens, TX, United States |
| Recall initiated | 2014-06-05 |
| Classified | 2014-09-24 |
| Reported by FDA | 2014-10-01 |
| Terminated | 2015-04-08 |
| Distributed | Nationwide (US) |
| Quantity | 3,783 units |
| Reason classes | packaging |
| Lot numbers | 11021364, 11027376, 11033757, 11034000, 11034387, 11034424, 11034914, 11034915, 11035965, 11035976, 11036453, 11038334, 11039525, 11041251, 11041518, 11044383, 11044868, 11045439, 11047511, 11049668, 11050693, 11052111, 11054199, 11054546, 11057890, 11059459, 11059468, 11059625, 11059627, 11060050, 11061874, 11067035 |
| Model numbers | 32101524 |
Product
UltraStream Chronic Hemodialysis Catheter Standard Kit; Model Number 32101524 (24 cm), 32101528 (28cm), 32101532 (32 cm), and 32101536 (36 cm) and 32102540 (40 cm). The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high flow rates at low arterial pressure.
Reason for recall
UltraStream Chronic Hemodialysis Catheter may develop cracks on the red (arterial) luer during attachment or manipulation.
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-2696-2014. 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.