Reported Jun 6, 2018 · Terminated
Radial Artery Catheterization Kit; Product Codes: ASK-04020-AH, ASK-04020-MIHS, ASK-04120-HF1
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?
- Radial Artery Catheterization Kit
- Product Codes
ASK-04020-AHASK-04020-MIHSASK-04120-HF1
- Lot codes and dates
- Lot NumbersProduct
- code ASK-04020-AH13F17B0102 13F17C0283 13F17F0221 13F17G0480 13F17J0045 13F17L0127
- Product code ASK-04020-MIHS13F17A0174 13F17F0139
- Product code ASK-04120-HF1
13F17C036013F17D003413F17E009313F17F046813F17G026913F17J010113F17K031113F17L0489
- 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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