Reported Feb 26, 2020 · Terminated
Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN
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 FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN
- Lot codes and dates
- Lot Number13F18K0740
- Amount recalled
- 205
This recall covers 20 products
The agency filed one notice per product. You are reading one of them; the other 19 are below.
7 more are in the archive.
Where it was sold
Why it was recalled
Product lidstock contains the incorrect expiration date for the product
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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