Reported Jun 6, 2018 · Terminated
Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R)…
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?
- Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features
- Product CodesASK-42703-PTJH and ASK-45703-PTJH
- Lot codes and dates
- Lot NumbersProduct
- Code ASK-42703-PTJH13F17A0168 13F17C0074 13F17D0339 13F17G0029 13F17G0453 13F17L0509
- Product code ASK-45703-PTJH13F17B0016 13F17C0089 13F17D0105 13F17F0062 13F17H0250 13F17K0220 13F17L0560
- Amount recalled
- 416,055 total products
This recall covers 76 products
The agency filed one notice per product. You are reading one of them; the other 75 are below.
63 more are in the archive.
Where it was sold
- Nationwide
- PR
Why it was recalled
Product sterility may be compromised due to unsealed packaging.
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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