Synchron CX4, CX5 and CX9 Pro Systems.
FDA Recall Z-0067-04 · Posted 2003-10-24
Recalling FirmBeckman Coulter Inc
Recall StatusTerminated
Product CodeJQP
Date Initiated2003-09-29
Date Terminated2004-04-05
Product Quantity351
Reason for Recall
Motor driver boards may contain wrong type of microchip which does not have obstruction detection feature.
Firm Action
Product Corrective Action letter was sent the week of 9/29/2003 by US MAIL with a fax back card.
Root Cause
Other
Distribution Pattern
Nationwide and Canada
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.