Reported Feb 19, 2020 · Terminated
EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-EXP
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 UR-05501-EXP
- Lot codes and dates
- Lots
71F19B075771F19D149371F19E234471F19G264071F19J057571F19C074871F19E019371F19G114671F19H212071F19K1689
- Lots
- 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.
Free recall alerts
Get alerted about new Arrow International Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.