Reported Oct 1, 2014 · Terminated

UltraStream Peel Away Kit; Model Numbers 32401524 (24 cm), 32401528 (28cm), 32401532 (32 cm), and 32401536 (36 cm) and…

Argon Medical Devices, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Argon Medical Devices, Inc · 1445 Flat Creek Rd · Athens, TX · 75751-5002

Is this the product you have?

  • UltraStream Peel Away Kit; Model Numbers 32401524 (24 cm), 32401528 (28cm), 32401532 (32 cm), and 32401536 (36 cm) and 32402540 (40 cm) The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high flow rates at low arterial pressure.
Lot codes and dates
  • Lot Numbers

    85 of 85 codes

    • 11030816
    • 11031844
    • 11032797
    • 11033587
    • 11033816
    • 11034388
    • 11035767
    • 11038234
    • 11038335
    • 11039565
    • 11041289
    • 11041994
    • 11043179
    • 11044967
    • 11045825
    • 11048504
    • 11049437
    • 11049775
    • 11050202
    • 11051294
    • 11054323
    • 11055558
    • 11057594
    • 11059629
    • 11061076
    • 11063899
    • 11067036
    • 11025361
    • 11030817
    • 11031845
    • 11032798
    • 11033391
    • 11033945
    • 11034347
    • 11035769
    • 11036779
    • 11038235
    • 11038990
    • 11040156
    • 11041290
    • 11044061
    • 11045091
    • 11046609
    • 11047537
    • 11049868
    • 11050802
    • 11053027
    • 11053781
    • 11054547
    • 11054548
    • 11055303
    • 11056428
    • 11059470
    • 11062800
    • 11067037
    • 11030950
    • 11032799
    • 11033588
    • 11034388
    • 11035770
Amount recalled
3,783 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

UltraStream Chronic Hemodialysis Catheter may develop cracks on the red (arterial) luer during attachment or manipulation.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Argon Medical Devices, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 8, 2015 · Data as of Sep 19, 6:48 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.