Reported Feb 19, 2020 · Terminated
EPIDURAL CATHETERIZATION KIT, Product Code BE-05400B-ETTEL
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?
- EPIDURAL CATHETERIZATION KIT, Product Code BE-05400B-ETTEL
- Lot codes and dates
- Lots71F19C0509 71F19G0116 71F19H1409 71F19J1840 71F19D2945 71F19G2238 71F19J0078
- Amount recalled
- 343,105 total
This recall covers 49 products
The agency filed one notice per product. You are reading one of them; the other 48 are below.
36 more are in the archive.
Where it was sold
Why it was recalled
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
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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