Device Recall AUTOMIX 33 의 리콜

Recall

57790

Class 2

Z-1385-2011

2011-01-27

2011-02-22

Terminated

United States

2012-02-16

USFDA

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97472

The automix compounder may not respond correctly to the key pressed by the operator using the keypad. the incorrect keypad response issue can occur both in manual data entry mode (std mode) and when entering order numbers to download from host software (man id mode). it is possible that an incorrect volume and/or an incorrect solution could be admixed into the final bag.

Baxter Healthcare Corp. sent Urgent Device Correction letters dated January 27, 2011, via first class mail to all affected customers. informing personnel that use Automix compounders to exercise care when entering data, and verify the accuracy of the keypad response. The accounts were requested to convey this information to all users of the Automix compounders, emphasizing the need to verify data accuracy each time the keypad is used. The accounts were also requested to complete the attached customer reply form listing the model and serial number of each of the Automix compounders at the facility and confirming their receipt of the letter, and fax it to Baxter at the number provided on the form. Any questions regarding the communication were directed to their local Baxter representative, and technical questions were directed to Baxter's Global Technical Services at 1-800-626-2667. After determining the root cause of the incorrect keypad responses, Baxter issued a follow-up correction letter on 4/27/11 outlining the recommended work practices to reduce fluid penetration into the Automix compounder keypad/control module.