c6000, Chemistry (Photometric, Discrete), for clinical use. - cobas e 601 module: Immunoassay Analyzer, Catalog Numbers: 04745922001, 05036348001, 05860652001, 04745922692, 05036348001 & 05036348692
FDA Recall Z-1268-2018 · Posted None
Advertisement
Recalling FirmRoche Diagnostics Corporation
Recall StatusTerminated
Product CodeJJE
Date Initiated2017-12-18
Date Terminated2019-04-09
Reason for Recall
Complaints have been received concerning questionable results on analyzers due to customers utilizing 13 sample tubes without tube adapters.
Firm Action
Roche Diagnostics Corporation issued Urgent Medical Device Correction (UMDC) notices and Fax Forms to their customers dated 12/18/2017 via UPS Ground (receipt required). Customers are encouraged to do the following Mandatory Steps to improve the vertical alignment and handling of 13 mm sample tubes and false bottom tubes:
FOR cobas e 411 & cobas e 601 analyzers and MODULAR ANALYTICS E 170 module:
1) Always use Roche rack cup adapters with 13 mm tubes
2) Ensure sample tubes are straight
FOR cobas e 411 disk system:
1) Always use 13 mm Sample Disk Tube Adapters (SDTAs) with 13 mm sample tubes.
2) Ensure sample tubes are straight.
3) Ensure 13 mm SDTAs are not exposed to direct sunlight.
4) If a larger diameter tube is left inserted in a 13 mm SDTA for more than 3 days, the adapter may become distorted. Do not insert smaller diameter tubes into distorted adapter as they may not align
correctly.
**All customers are encouraged to DISCARD Analyzer Bulletin 10-009U3.
Follow the care and handling instructions for using adapters as outlined in this Urgent Medical Device Correction (UMDC) and complete & return the UMDC fax form via fax to 1-877-271-1472
Root Cause
Labeling False and Misleading
Distribution Pattern
US Nationwide
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement