FDA-Device2014-10-22Class II

Multi-Lumen Central Venous Catheterization Kit

Arrow International Inc
Hazard

Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct expiration date.

Sold states
US Distribution including the states of MD, NC , LA , IN , OH, KY, CA , PA , NY and NV.
Affected count
65
Manufactured in
2400 Bernville Road, N/A, Reading, PA, United States
Products
Multi-Lumen Central Venous Catheterization Kit

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0076-2015

Don't want to check this manually?

We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Get the Sunday Brief