Device Recall COULTER LH750 Analyzer 의 리콜

Recall

57990

Class 2

Z-1953-2011

2011-01-31

2011-04-12

Terminated

United States

2012-09-25

USFDA

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97922

This recall was initiated because beckman coulter identified a problem with some date fields that are transmitted to the laboratory information system (lis). starting jan 1, 2011, the date fields will transmit as a blank field to the lis if the year is greater than 2010. the following dates are affected: run date, control expiration date, date of birth (for individuals born in 2011 or later), a.

The firm, Beckman Coulter, sent an "URGENT: PRODUCTION CORRECTION" letter dated January 31, 2011 with attached PCA Response Form (via US Postal Service for US Customers) to all customers who purchased the Coulter LH 750 Analyzer, Coulter LH 780 Analyzer, Coulter LH 500 Series System, and Coulter GEN S System. The letter describes the product, problem and actions to be taken. The customers were instructed to work with their US vendor to assess how this affects their laboratory. The actions they choose are dependent on the configuration of their LIS. ACTION FOR ISSUE 1: Use Sample Drawn Date and Date of Birth information available at your LIS in lieu of the analyzer transmitted fields BIRTH and UDATE. Use the current date when the results are received at the LIS in lieu of the transmitted Run Date [DATE]. Print results from the Workstation to keep a copy of the analysis date on the analyzer, if necessary. Use the control expiration date from the analyzer display or printout. ACTION FOR ISSUE 2: If you use the LIS 1G1 transmission format, use the General Information group field names in place of the Retic Parameter group field names to identify each reticulocyte run (see Table in Issue 2 section). Check with your LIS vendor to determine if it is possible to switch to the LH 750 Workstation transmission format. Format requirements are LIS driver specific. For patients with Dates of Birth in 2011 for both Issue 1 and Issue 2, results should be reviewed to determine if decision rules or age-related limits sets were triggered inappropriately. RESOLUTION These issues will be corrected in a future software release for the LH Series products. The GEN¿¿S product has been discontinued; no software revisions will be forthcoming for the GEN¿¿S product line. Customers were also instructed to complete and return the PRODUCT CORRECTION RESPONSE FORM via fax to 786-639-7500/7501/7502/7503/7504; mail to Beckman Coulter, Inc., Attn: Regulatory Affairs Mail Code 310B06, 11