Atlas FDA

AU680 Chemistry Analyzers, Reference No. B04779 The AU series are automated, clinical chemistry analyzers that measure a

FDA device recall Z-2309-2016 · posted 2016-08-01 · Terminated

Recall details

Recalling firm
Beckman Coulter Inc.
Reason for recall
Beckman coulter has received complaints regarding leaking and cracked C cups. When the cup cracks, coolant can leak onto the connectors of the Printed Circuit Boards (PCB) in the analyzer, resulting in a short-circuit causing the instrument to go into a stop mode.
Action taken
In March 2011, the material and molding process of the Coolant cup (C cup) was changed. BEC did not issue a customer notification letter, as we do not believe that a notificationletter was either warranted or of any potential use or value to our customers, because the coolant cup (C cup) is an internal component that only a BEC Field Service Engineer (FSE) can access and inspect i.e., the C cup is not in a customer-accessible part of the analyzer. Thus, there are no specific actions the customer could take to inspect, identify, or mitigate the potential for a crack or leakage of the C cup. For questions regarding this recall call 714-961-4933.
Root cause
Nonconforming Material/Component
Status
Terminated
Product code
JJE
Quantity affected
3,084 units total (713 units in US)
Distribution
Worldwide Distribution - US (nationwide (including Guam and Puerto Rico), and Internationally to Albania, Algeria, Australia, Austria, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Bo
Date initiated
2015-07-30
Date posted
2016-08-01
Date terminated
2017-02-15
Location
Brea, CA

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.

Related 510(k) clearances

RecordFirmDate
OLYMPUS AU600 CLINICAL CHEMISTRY ANALYZER (K961274)Olympus America, Inc.1996-07-05