Recall Z-2291-2011

Baxter Healthcare Corp. · initiated March 29, 2011

Terminated

Product

LOGIX Order Entry (OE) Software, all versions, catalog 2M8410; Baxter Healthcare, Deerfield, IL 60015; The software is included in a number of Baxter's pharmacy compounders. The software assists the pharmacist in management of compounding, creating and authorizing nutritional solutions intended for IV administration.

Codes / lots: catalog 2M8410, all software versions

Reason for recall

The LOGIX OE automated backup does not retain the three most recent backup files and instead will only retain the last three backups of the previous year. The software stores backup files in numeric order rather than chronological date order.

FDA-determined cause: Software design

Action taken

Baxter Healthcare Corp. sent an URGENT DEVICE CORRECTION letter dated March 29, 2011, via first class mail to all affected customers. The letter identified the product, the problem and the action to be taken by the customer. It was discovered there is an issue with the LOGIX OE automated backup not retaining the three most recent backup files and instead will only retain the last three backups of the previous year. The accounts were requested to turn off the automated backup function on the LOGIX OE Software, and perform manual backups following the instructions included in the Urgent Device Correction letter, and retain a copy of the letter at each computer on which LOGIX OE Server is installed. The customer were also requested to complete the attached customer reply form and fax it to Baxter at the number provided on the form. Any questions regarding the communication were directed to Baxter's Medical Information Services at 1-800-422-2751.

Details

Recall number
Z-2291-2011
Initiated
March 29, 2011
Posted by FDA
May 25, 2011
Terminated
January 5, 2017
Product code
LHI – Set, I.V. Fluid Transfer
Quantity
84 units
Distribution
Worldwide Distribution -- USA including Puerto Rico, and the country Canada.
Recalling firm
Baxter Healthcare Corp., Round Lake, IL

Official FDA recall record