Z-2087-2016 Class II Terminated
FDA device recall Z-2087-2016 was initiated by Siemens Healthcare Diagnostics Inc. on May 11, 2016 and is designated Class II. Reason for recall: Premature bucket failures The recall status is terminated (terminated Apr 27, 2018). Affected quantity: 487.
Recall Details
- Product Type
- Devices
- Report Date
- Jul 6, 2016
- Initiation Date
- May 11, 2016
- Termination Date
- Apr 27, 2018
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 487
Product Description
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.
Reason for Recall
Premature bucket failures
Distribution Pattern
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.
Code Information
All serial numbers are affected.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2087-2016
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026