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Type of Product Medical Device
TGA Recall Reference RC-2014-RN-00562-1
Product Name/Description Ultrasonic Transducer Kits used with the Access Family of Immunoassay Systems. An in vitro diagnostic medical device (IVD)
Recall Action Level Hospital
Recall Action Classification Class II
Recall Action Commencement Date 21/05/2014
Responsible Entity Beckman Coulter Australia Pty Ltd
Reason/Issue Beckman Coulter has determined that some Ultrasonic Transducer Kits were potentially assembled with incorrect mounting screws. One of these transducers may have been installed on the system during a recent instrument repair. Over time the screws can become loose if a combination of correct and incorrect screws are used and possibly cause Incorrect probe wash, splashing in the reaction vessels (RV), incorrect particle suspension in the reagent pack, or incorrect RV mix due to alignment of the probe to wash tower/RV leading to assay imprecision. This may cause erraneous but believable results and/or delay of results due to transducer alignment error.
Recall Action Recall for Product Correction
Recall Action Instructions Users are advised to review historical QC data and System Check results since the transducer was installed for any indication of a potential problem and determine whether a review of patient test results is warranted. A service representative will be contacting users to schedule a service visit to confirm that their transducer is properly installed.
Contact Information 1800 060 881 - Beckman Coulter Customer Support Centre