Reported Jun 6, 2018 · Terminated
Arterial Catheterization Kit; Product Codes: ASK-04020-DH
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?
- Arterial Catheterization Kit
- Product CodesASK-04020-DH
- Lot codes and dates
- Lot Numbers
13F17B030713F17D007013F17E041713F17G001213F17G050813F17H042113F17L015513F17L0478
- Lot Numbers
- 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.
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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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