Reported Feb 19, 2020 · Terminated
EPIDURAL CATHETERIZATION KIT, Product Code BE-080180-CHH
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-080180-CHH
- Lot codes and dates
- Lots71F19D0608 71F19F1570 71F19H2423 71F19K1108 71F19E2537 71F19G2485 71F19J1513
- 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.
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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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