Reported Feb 19, 2020 · Terminated
FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B
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?
- FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B
- Lot codes and dates
- Lots71F19E2457 71F19G0988 71F19H1281 71F19K2009 71F19F1658 71F19G2371 71F19J1079
- Amount recalled
- 343105 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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