Reported Apr 29, 2026 · Ongoing
Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 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?
- Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen
- CVC Kit REF ASK-45854-PUPM1 UDI code(01)10801902159578(17)270531(11)251205(10)33F25M0011 The Arrowg+ard technology is intended to provide protection against catheter-related bloodstream infections (CRBSIs). It is not intended to be used as a treatment for existing infections nor is it indicated for long-term use (> 30 days). Clinical effectiveness of the Arrowg+ard Blue Plus catheter in preventing CRBSIs compared to the original Arrowg+ard Blue¿ catheter has not been studied
- Lot codes and dates
- Product CodeASK-45854-PUPM1
- UDI code(01)10801902159578(17)270531(11)251205(10)33F25M0011
- Batch Number33F25M0011
- Product CodeASK-45703-MGH
- UDI code(01)10801902223675(17)261231(11)251209(10)33F25L0143
- Batch Number33F25L0143
- Product CodeASK-42854-MGH
- UDI code(01)10801902223668(17)261231(11)251210(10)33F25L0144
- Batch Number33F25L0144
- Product CodeASK-45854-MGH
- UDI code(01)10801902223699(17)261231(11)251209(10)33F25L0145
- Batch Number33F25L0145
- Amount recalled
- 5
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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