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Siemens Healthcare Diagnostics, Inc. recalls ADVIA Centaur (including refurbished) Professional use in a laboratory for in vitro diagnostic tests.
Recalled December 31, 2014 · FDA recall Z-0859-2015 · Siemens Healthcare Diagnostics
Hazard
A slight crack of the tubing at the connecting fitting on the reservoir connector assembly may occur due to mechanical stress. · FDA Class II
Units
10,515 units total
Sold at
Nationwide Distribution including PR and the states of AK, AL, AR, AZ, CA, CO, CT, MD, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY.
Description
A slight crack of the tubing at the connecting fitting on the reservoir connector assembly may occur due to mechanical stress.
Product
ADVIA Centaur (including refurbished) Professional use in a laboratory for in vitro diagnostic tests.
Manufacturer(s)
Siemens Healthcare Diagnostics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →