Reported Jun 24, 2026 · Ongoing
Description/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC; AHDC KIT: 3-L 12 FR X 20 CM/AK-15123-PCDC; AHDC KIT: 3-L 12…
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?
7 of 7 products
| # | Product as published |
|---|---|
| 1 | Description/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC |
| 2 | AHDC KIT: 3-L 12 FR X 20 CM/AK-15123-PCDC |
| 3 | AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-XP1A |
| 4 | AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XP1A |
| 5 | AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XPN1A |
| 6 | AHDC AGB U-BEND KIT: 2-L 12 FR X 20 CM/CDC-25122-XN1A-U |
| 7 | LBCVC AGB KIT: 3-L 12 FR X 16 CM/CDC-22123-XN1A |
- Lot codes and dates
7 of 7 products
Products covered by this recall # Barcodes Product as published 1 1080190219327510801902168471AK-12123-PCDC/10801902193275, 10801902168471/33F24J0419, 33F25B0015, 33F25F0022, 33F25G0482, 33F25J0029, 33F25K0268, 33F26B0056, 33F24E0175 2 108019021864991080190219327510801902168532AK-15123-PCDC/10801902186499, 10801902193275, 10801902168532/33F24G0140, 33F24J0449, 33F24M0074, 33F25B0040, 33F25J0604, 33F24A0767 3 108019021932753080190211182210801902213430CDC-15123-XP1A/10801902193275, 30801902111822, 10801902213430/33F25D0438, 33F25E0649, 33F25H0579, 33F25J0313, 33F26B0161, 33F26C0198, 33F24D0355 4 1080190219327540801902111867CDC-16123-XP1A/10801902193275, 40801902111867/33F25D0612, 33F25G0291, 33F25H0578, 33F26C0190, 33F24L0469 5 1080190219327510801902196498CDC-16123-XPN1A/10801902193275, 10801902196498/33F25J0113, 33F24D0974 6 10801902193275CDC-25122-XN1A-U/10801902193275/33F25J0114, 33F25B0621 7 50801902123515CDC-22123-XN1A/50801902123515/33F24D0928 - Amount recalled
- 4,270
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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