RecalledThisWeek Search
Medium risk Drugs & MedicationsClass II

ARROW INTERNATIONAL, LLC Recall

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)2512

Updated March 11, 2026

ARROW INTERNATIONAL, LLC is recalling 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)2512. Hazard: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Is the ARROW INTERNATIONAL, LLC recalled? Yes. This product was recalled by FDA on March 11, 2026. Details below.

What is recalled

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.

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Brands affected

ARROW INTERNATIONAL, LLC
Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-1916-2026
Classification
Class II
Recalled
March 11, 2026
Read the official notice

Get free recall alerts

New Drugs & Medications recalls, the moment they post.

Free forever. Unsubscribe anytime. We never sell your data.

More Drugs & Medications recalls