Reported Apr 29, 2026 · Ongoing
MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code:…
Arrow International, LLC
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, LLC · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437
Is this the product you have?
- MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr
- Catheters REF ASK-11142-LC2 UDI code(01)10801902206807(17)270531(11)251211(10)33F25M0670 The MAC Multi-Lumen Central Venous Access Device permits short-term (<30 days) venous access and catheter introduction to the central circulation
- Lot codes and dates
- Product CodeASK-11142-LC2
- UDI code(01)10801902206807(17)270531(11)251211(10)33F25M0670
- Batch Number33F25M0670
- Amount recalled
- 90
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
Why it was recalled
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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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