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Recall Observatory FDA recall evidence

Device product

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

Z-1767-2017

March 17, 2017

Class II

Product summary

Firm
Smiths Medical ASD Inc.
Event
Event 76749
Status
Terminated
Classification
Class II
Quantity
38,415 (38145 US; 2268 OUS)
Official record key
device-enforcement:Z-1767-2017

Official wording

Reason: 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.

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

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.