Reported Jun 24, 2026 · Ongoing
Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000
Arrow International, LLC
High riskUsing this product could cause serious injury, illness or death — stop using it now.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, LLC · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437
Is this the product you have?
- Description/REFPERITONEAL
- LAVAGE CATH KIT8FR/AK-09000
- Lot codes and dates
- REF(Material)/UDI-DI/Lot(Batch)
AK-09000/308019021217221080190219327520801902121756/33F24B017833F24C009733F24E033633F24F031133F24G033533F24K010133F24L079533F25E091933F25G046733F25G075833F25H072233F25J046833F25L046333F26A038933F24A0368
- REF(Material)/UDI-DI/Lot(Batch)
- Amount recalled
- 7560
This recall covers 35 products
The agency filed one notice per product. You are reading one of them; the other 34 are below.
22 more are in the archive.
Where it was sold
Why it was recalled
Stop using this product now
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Using this product could cause serious injury, illness or death — stop using it now.
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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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