ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 REF ASK-04020-EUH2 UDI code: (01)10801902213379(17)270731(11)251218(10)33F25J0869 REF ASK-04020-FMC UDI code: (01)10801902212099(17)270731(11)251218(10)33F25J0870 REF ASK-04020-MMC UDI code: (01)10801902117769(17)271130(11)251211(10)33F25J0880 The Arrow Arterial Catheterization Device permits access to the peripheral arterial circulation or to other small vessels.
Class II
- Recalling firm
- ARROW INTERNATIONAL, LLC
- Reason for recall
- Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
- Distribution pattern
- U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.
- State
- NC
- Status
- Ongoing
- Recall number
- Z-1911-2026
- Recall initiated
- March 11, 2026
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