Z-0096-2017 Class II Terminated
FDA device recall Z-0096-2017 was initiated by Roche Diagnostics Operations, Inc. on Jul 15, 2016 and is designated Class II. Reason for recall: Roche has received four reports of injury caused by the sharp edge of the center guide rail of an analyzers sample rack tray. The cleaning procedure for the sample rack tray has been revised to… The recall status is terminated (terminated Jun 5, 2017). Affected quantity: 9014 in total.
Recall Details
- Product Type
- Devices
- Report Date
- Nov 2, 2016
- Initiation Date
- Jul 15, 2016
- Termination Date
- Jun 5, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9014 in total
Product Description
cobas 6000 Series system c6000, Chemistry (Photometric, Discrete), for clinical Use. Modular e601: Immunoassay Analyzer Product Usage: The cobas p501/p701 instrument stores primary and secondary sample tubes. The tubes are stored in a controlled, refrigerated sample store. Automatic retrieval for add-on testing is possible at any time. Expired samples are disposed of automatically when their storage time has elapsed. The instrument is intended as accessory for diagnostic use.
Reason for Recall
Roche has received four reports of injury caused by the sharp edge of the center guide rail of an analyzers sample rack tray. The cleaning procedure for the sample rack tray has been revised to clarify the cleaning process.
Distribution Pattern
US Nationwide Distribution
Code Information
Not applicable
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0096-2017
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026