Reported Apr 17, 2019 · Terminated
Arrow¿ Two-Lumen Central Venous Catheterization Kit with Blue FlexTip¿ Catheter Product Code: AH-11802 (OUS) 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 Kit with Blue FlexTip¿
- Catheter Product CodeAH-11802 (OUS)
- GTN00801902026132
- Lot codes and dates
- Lot Numbers
71F14E069671F14K065871F15E049371F15L062171F14E154171F14K168371F15F009071F15M078771F14F115471F14L071971F15H057471F16A027871F14H047471F14M137571F15H150371F16B005471F14H121571F15A002571F15J057071F16B130671F14J085271F15A159271F15J209871F14J188971F15D146071F15L0153
- Lot Numbers
- Amount recalled
- None (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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