RecallDepth

Instrument Manager -Software Versions 8.05, 8.06, 8.07, 8.08, and 8.09. It is a stand-alone software package that provides connectivity between laboratory instruments and Laboratory Information Systems, aiding the flow of laboratory information, including test orders and results, specimen information, and patient information. Instrument Manager also provides data management functions that aid in the interpretation and management of laboratory results. The Instrument Manager software is put on a CD which is distributed in a box. User documentation consists of user manuals, PDF copies of which are on the CD Intended to be used by trained laboratory personnel as an aid in laboratory instrument interfacing and laboratory data management.

This recall has been terminated (originally issued October 21, 2011).

Company
Data Innovations, Inc.
Recall Initiated
May 11, 2009
Posted
October 21, 2011
Terminated
October 25, 2011
Recall Number
Z-0083-2012
Quantity
188
Firm Location
South Burlington, VT
Official Source
View on FDA website ↗

Reason for Recall

The "previous result" retrieved from the Specimen Management Database may not be the most recent "previous result".

Distribution

USA (nationwide) and the country of Canada.

Lot / Code Info

S/W Versions 8.05, 8.06, 8.07, 8.08 and 8.09.

Root Cause

Software design

Action Taken

Data Innovations sent an "IMPORTANT PRODUCT NOTICE" dated May 11, 2009 to all affected customers. The letter describes the product, problem, and actions to be taken by the customers. The letter offers temporary workarounds for customers to use until corrected versions of the software is complete. Versions of the corrections will be provided on a staggered schedule. Customers will be notified by e-mail. Questions regarding this notice are directed to Support at 802-658-1955.

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