Reported Apr 29, 2026 · Ongoing
ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-42802-PLH 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?
4 of 4 products
| Model / number | Barcodes | Product as published |
|---|---|---|
ASK-42802-PLH | 10801902133110 | UDI code: (01)10801902133110(17)261231(11)251211(10)33F25L0140 |
ASK-45703-MGH | 10801902223675 | UDI code: (01)10801902223675(17)261231(11)251209(10)33F25L0143 |
ASK-42854-MGH | 10801902223668 | UDI code: (01)10801902223668(17)261231(11)251210(10)33F25L0144 |
ASK-45854-MGH | 10801902223699 | UDI code: (01)10801902223699(17)261231(11)251209(10)33F25L0145 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-42802-PLH
- UDI code(01)10801902133110(17)261231(11)251211(10)33F25L0140
- Batch Number33F25L0140
- 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
- 395
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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