Z-1767-2017 Class II Terminated

Recalled by Smiths Medical ASD Inc. — Minneapolis, MN

Recall Details

Product Type
Devices
Report Date
April 19, 2017
Initiation Date
March 17, 2017
Termination Date
July 3, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
38,415 (38145 US; 2268 OUS)

Product Description

CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.

Reason for Recall

Smiths Medical has become aware that the drawing on the Instructions for Use (IFU) on certain yellow striped CADD¿ Administration Sets (part number 21-7339-24), incorrectly represent the actual filter size of the product. Although the text description on the IFU correctly identifies the product to include a 0.2 micron filter, the illustration on the IFU identifies the filter size as 2.0 microns.

Distribution Pattern

US:AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WV, WY. OUS: Canada

Code Information

46X817, 46X829, 46X899, 46X828, 46X896, 46X990, 46X831, 46X897, 46X1001.