Diagnost 97
FDA Recall Z-1213-03 · Posted 2003-09-11
Recall StatusTerminated
Product CodeIZZ
Date Initiated2003-08-10
Date Terminated2005-01-13
Product Quantitysee above
Reason for Recall
Potential for table to move by itself
Firm Action
The firm issued a letter dated 8/10/03 informing the consignees of the error and advising that a service employee will be visiting each site for software upgrade.
Root Cause
Other
Distribution Pattern
The firm distributed devices to hospitals and medical centers located throughout the U.S.
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.