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.

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
Affected products (lot / model / serial): Product Code: ASK-11142-LC2 UDI code: (01)10801902206807(17)270531(11)251211(10)33F25M0670 Batch Number: 33F25M0670
Units affected: 90
Distribution pattern: U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.
Firm location: Morrisville, NC, United States
Recall type: Voluntary: Firm initiated
How the firm notified customers: Letter
Product type: Devices
Status: Ongoing
Recall number: Z-1916-2026
Recall initiated: March 11, 2026
FDA classification date: April 22, 2026
FDA report date: April 29, 2026
FDA event ID: 98618
Last updated on HTM Vibe: July 24, 2026