Section R. 325.9082 - Reportable informationRule 2.
(1) Reportable information pertains to the analysis of blood samples submitted to clinical laboratories and the results from portable blood lead analyzers.(2) Upon initiating a request for blood lead analysis, the physician/provider or user ordering the blood lead analysis shall collect the following information: (a) All of the following information with respect to the individual tested:(iii) The individuals ethnic origin.(iv) The individuals race.(vi) Address, including county.(viii) Social security number and Medicaid number, if applicable.(ix) If the individual is a minor, the name of a parent or guardian.(x) If the individual is an adult, the name of his or her employer.(xi) A secondary contact for the individual tested or, if the individual is a minor, a secondary contact for the individuals parent or guardian, including, to the extent available, name and phone number of the secondary contact.(b) The date of the sample collection.(c) The type of sample, either capillary or venous.(d) The physicians/providers or users name, name of practice or agency, if applicable, telephone number, fax number, email address, and mailing address.(3) The information collected in subrule (2) of this rule must be submitted with the sample for analysis to a clinical laboratory that performs blood lead analysis or a user of a portable blood lead analyzer.(4) Upon receipt of the blood sample for lead analysis, the clinical laboratory or user of a portable blood lead analyzer shall collect the following additional information: (a) The name, address, and phone number of the laboratory or testing entity.(b) The date of analysis.(d) The results of the blood lead analysis in micrograms of lead per deciliter of whole blood. If the result is below the limit of detection, report as less than the laboratorys limit of detection for that analytical procedure.Mich. Admin. Code R. 325.9082
1997 AACS; 2015 AACS; 2020 MR 3, Eff. 2/7/2020