Reported Apr 17, 2019 · Terminated

Arrow¿ Two-Lumen Central Venous Catheterization Set with Blue FlexTip¿ Catheter Product Code: CD-10802 GTN:…

Arrow International 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: Arrow International Inc · 2400 Bernville Rd · Reading, PA · 19605-9607

Is this the product you have?

  • Arrow¿ Two-Lumen Central Venous Catheterization Set with Blue FlexTip¿
  • Catheter Product CodeCD-10802
  • GTN00801902015396
Lot codes and dates
  • Lot NumbersUS: 71F15J1055 71F15K0223 71F15D1461 71F18A1856
  • Worldwide

    78 of 78 codes

    • 71F14H0908
    • 71F15K0223
    • 71F16M1878
    • 71F18A0343
    • 71F14J0958
    • 71F15L0155
    • 71F17A0524
    • 71F18A1856
    • 71F14J1954
    • 71F15L1514
    • 71F17A1118
    • 71F18B0295
    • 71F14J1955
    • 71F15M0771
    • 71F17A1119
    • 71F18B3053
    • 71F14K1117
    • 71F16A0286
    • 71F17A2452
    • 71F18C0752
    • 71F14L0040
    • 71F16A1142
    • 71F17C0184
    • 71F18C1686
    • 71F14L0813
    • 71F16B0097
    • 71F17C0408
    • 71F18C2250
    • 71F14M0892
    • 71F16B1126
    • 71F17C2294
    • 71F18C3030
    • 71F14M1389
    • 71F16B2212
    • 71F17C2749
    • 71F18C3042
    • 71F15A0039
    • 71F16C1127
    • 71F17D0329
    • 71F18D2222
    • 71F15D1461
    • 71F16D1063
    • 71F17E1237
    • 71F18E1357
    • 71F15E1320
    • 71F16E0976
    • 71F17E2316
    • 71F18E1753
    • 71F15F1005
    • 71F16F0403
    • 71F17F0829
    • 71F18F2625
    • 71F15F1955
    • 71F16F1512
    • 71F17G1171
    • 71F18G0263
    • 71F15G0461
    • 71F16G0246
    • 71F17G1628
    • 71F18G2183
Amount recalled
45 eaches total (US)

This recall covers 2 products

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

Where it was sold

Why it was recalled

The product lidstock contains a labelling error. The lidstock states the incorrect priming volume. The priming volumes printed on the extension lines are correct

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.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 4, 2020 · Data as of Sep 19, 5:38 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.