TITLE 35: ENVIRONMENTAL PROTECTION
SUBTITLE F: PUBLIC WATER SUPPLIES
CHAPTER I: POLLUTION CONTROL BOARD
PART 611 PRIMARY DRINKING WATER STANDARDS
SECTION 611.805 REPORTING AND RECORDKEEPING FOR GWS SUPPLIERS


 

Section 611.805  Reporting and Recordkeeping for GWS Suppliers

 

a)         Reporting.  In addition to the requirements of Section 611.840, a GWS supplier regulated under this Subpart S must provide the following information to the Agency:

 

1)         A GWS supplier conducting compliance monitoring under Section 611.803(b) must notify the Agency any time the supplier fails to meet any Agency-specified requirements including minimum residual disinfectant concentration, membrane operating criteria or membrane integrity, and alternative treatment operating criteria, if operation in accordance with the criteria or requirements is not restored within four hours.  The GWS supplier must notify the Agency as soon as possible, but in no case later than the end of the next business day.

 

2)         After completing any corrective action under Section 611.803(a), a GWS supplier must notify the Agency within 30 days after completion of the corrective action.

 

3)         If a GWS supplier subject to the requirements of Section 611.802(a) does not conduct source water monitoring under Section 611.802(a)(5)(B), the supplier must provide documentation to the Agency within 30 days after the total coliform-positive sample that it met the Agency criteria.

 

b)         Recordkeeping.  In addition to the requirements of Section 611.860, a GWS supplier regulated under this Subpart S must maintain the following information in its records:

 

1)         Documentation of corrective actions.  Documentation must be kept for at least ten years.

 

2)         Documentation of notice to the public as required under Section 611.803(a)(7).  Documentation must be kept for at least three years.

 

3)         Records of decisions under Section 611.802(a)(5)(B) and records of invalidation of fecal indicator-positive groundwater source samples under Section 611.802(d).  Documentation must be kept for at least five years.

 

4)         For a consecutive system supplier, documentation of notification to the wholesale systems of total coliform-positive samples that are not invalidated under Section 611.1053.  Documentation must be kept for at least five years.

 

5)         For a supplier, including a wholesale system supplier, that is required to perform compliance monitoring under Section 611.803(b), the following information:

 

A)        Records of the supplier-specified, Agency-approved minimum disinfectant residual.  Documentation must be kept for at least ten years;

 

B)        Records of the lowest daily residual disinfectant concentration and records of the date and duration of any failure to maintain the Agency-prescribed minimum residual disinfectant concentration for a period of more than four hours.  Documentation must be kept for at least five years; and

 

C)        Records of supplier-specified, Agency-approved compliance requirements for membrane filtration and of parameters specified by the supplier for Agency-approved alternative treatment and records of the date and duration of any failure to meet the membrane operating, membrane integrity, or alternative treatment operating requirements for more than four hours.  Documentation must be kept for at least five years.

 

BOARD NOTE:  Derived from 40 CFR 141.405.

 

(Source:  Amended at 47 Ill. Reg. 7556, effective May 16, 2023)