Home / Recalls / Medical Devices
Siemens Healthcare Diagnostics Inc. recalls Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or 10444807 or 10706836) Aptio Centrifuge Module (10
Recalled July 6, 2016 · FDA recall Z-2087-2016 · Siemens Healthcare Diagnostics
Hazard
Premature bucket failures · FDA Class II
Units
487
Sold at
Nationwide: AL, AR, AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, PA, SC, SD, TN, TX, VA, WA, WI, WV.
Description
Premature bucket failures
Product
Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or 10444807 or 10706836) Aptio Centrifuge Module (10703032 or 10713761) FlexLab High Throughput Centrifuge Module (11171747) FlexLab and Aptio Centrifuge Module (10628157 or 11266581): Used to separate substances according to their densities.
Manufacturer(s)
Siemens Healthcare Diagnostics Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →