ARROW INTERNATIONAL, LLC recalls PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)2

Recalled April 29, 2026 · FDA recall Z-1912-2026 · ARROW INTERNATIONAL

Hazard

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured · FDA Class II

Units

115

Sold at

U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.

Description

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

Product

PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 The Arrow¿ percutaneous sheath introducer permits venous access and catheter introduction to the central circulation.

Manufacturer(s)

ARROW INTERNATIONAL, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →