Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
1) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit 2) Recalled by Arrow International Inc Due to Arrow International is recalling the affected product because...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Arrow International Inc directly.
Affected Products
1) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit 2) ARROWg+ard Blue PSI Kit 3) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit 4) ARROWg+ard Blue PSI Kit The MACTM two-Lumen Central Venous Access Device with ARROWg+ard Blue permits venous access and catheter introduction to the central circulation. It may be inserted into the jugular, subclavian, or femoral veins
Quantity: 27,485 untis distributed in U.S., 4,371 units distributed internationally
Why Was This Recalled?
Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Arrow International Inc
Arrow International Inc has 431 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report