Home / Recalls / Medical Devices
Roche Diagnostics Corporation recalls cobas p 501 post-analytical units, Part Number 05158494001. For diagnostic sample storage and retrieval.
Recalled July 10, 2019 · FDA recall Z-1927-2019 · Roche Diagnostics
Hazard
There is a potential for the tray input flap on the post analytical units to become loose, potentially detaching from the instrument. · FDA Class III
Units
4 units
Sold at
US Nationwide Distribution in the states of AL, CA, FL, IA, IL, KY, MD, OR & PA
Description
There is a potential for the tray input flap on the post analytical units to become loose, potentially detaching from the instrument.
Product
cobas p 501 post-analytical units, Part Number 05158494001. For diagnostic sample storage and retrieval.
Manufacturer(s)
Roche Diagnostics Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →