2024 -- H 7939 | |
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LC005400 | |
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STATE OF RHODE ISLAND | |
IN GENERAL ASSEMBLY | |
JANUARY SESSION, A.D. 2024 | |
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A N A C T | |
RELATING TO COMMERCIAL LAW -- GENERAL REGULATORY PROVISIONS -- | |
UNFAIR SALES PRACTICES | |
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Introduced By: Representative Alex D. Marszalkowski | |
Date Introduced: March 05, 2024 | |
Referred To: House Corporations | |
It is enacted by the General Assembly as follows: | |
1 | SECTION 1. Chapter 6-13 of the General Laws entitled "Unfair Sales Practices" is hereby |
2 | amended by adding thereto the following section: |
3 | 6-13-22. Continuous glucose monitors. |
4 | (a) Definition. For purposes of this section, "glucose monitor" means a device designed to |
5 | be placed upon or into a person for the purpose of monitoring and recording blood glucose (sugar) |
6 | levels in a person with diabetes mellitus. Said device consists of a sensory unit which monitors |
7 | glucose levels and transmits readings to another (receiving) device. The receiving unit shows the |
8 | user current glucose levels as well as past levels and calculates possible levels, warning user of low |
9 | glucose levels that pose a safety risk to the individual user and also to the general public due to the |
10 | possibility of the user becoming unconscious. |
11 | (b) It shall be unlawful for any retailer, to sell within this state, any glucose monitors |
12 | without having a replacement policy for glucose monitors that fail or are defective and any sensors |
13 | thereto that provides for an immediate, point of sale replacement or replacement within twenty- |
14 | four (24) hours at no charge to the consumer for any glucose monitors sold by the retailer. |
15 | (c) Failure of the glucose monitor shall include the following defects: |
16 | (1) Failure of the sensor unit to adhere to an individual due to the absence of adhesive; |
17 | (2) Failure of the sensor to adhere upon placement of the device to the individual; |
18 | (3) Failure of probe to enter the skin of the person and enter the subcutaneous tissue, |
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1 | rendering the device unable to function; |
2 | (4) Failure to adhere to the individual under normal operating conditions and under normal |
3 | daily use and activities within the intended usage time of the sensor unit; and |
4 | (5) Failure of the device to communicate with a receiver for the following reasons: |
5 | (i) The sensor claims to have been scanned by another receiving device and will not work |
6 | with the intended receiver; |
7 | (ii) The scanner prematurely stops working prior to its intended end of usage time, claiming |
8 | it has reached its intended usage time but has not; |
9 | (iii) The electronics malfunction thus rendering the device inoperable, including expired |
10 | battery; and |
11 | (iv) The receiving device fails due to electronic malfunction or the inability to be able to |
12 | recharge the battery. |
13 | (d) Retailers inventory. Retailers of glucose monitors shall maintain a sufficient inventory |
14 | of the monitors or have sufficient replacement vendors to enable replacement within twenty-four |
15 | (24) hours to any customer who has purchased a glucose monitor from the retailer. Any retailer |
16 | unable to meet the immediate replacement request requirement shall, upon the valid request for |
17 | replacement of a defective glucose monitor: |
18 | (1) Obtain a replacement within twenty-four (24) hours of the request by the consumer; |
19 | (2) Arrange for the delivery of a replacement glucose monitor to the consumer within |
20 | twenty-four (24) hours; or |
21 | (3) Inform and direct the customers to a location where a replacement glucose monitor may |
22 | be obtained with the cost of the monitor being the responsibility of the retailer who sold the |
23 | defective glucose monitor. |
24 | (e) Notice. All retailers of glucose monitors shall display at the point of sale location a copy |
25 | of this section of law and a sign explaining the customer's rights to a replacement glucose monitor |
26 | pursuant to this section and the contact information for the customer protection division of the |
27 | attorney general's office. |
28 | (f) Reporting. Retailers affected by the provisions of this section shall annually report to |
29 | the department of health: |
30 | (1) The total number of glucose monitoring devices returned to their store; |
31 | (2) The total number of glucose monitoring devices returned by the retailer to the |
32 | manufacturers; |
33 | (3) The number of replacement glucose monitors provided by the manufacturer; and |
34 | (4) The total amount of time spent replacing the glucose monitors. |
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1 | (g) Exemptions. The provisions of the section shall not apply to: |
2 | (1) Any device that receives signals including, but not limited to, cell phones; and |
3 | (2) Any damage to a glucose monitor caused by misuse or mistreatment. |
4 | (h) Penalties. Any person who violates the provisions of this section shall be guilty of a |
5 | misdemeanor and shall pay a fine of five hundred dollars ($500). |
6 | SECTION 2. This act shall take effect on January 1, 2025. |
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LC005400 | |
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EXPLANATION | |
BY THE LEGISLATIVE COUNCIL | |
OF | |
A N A C T | |
RELATING TO COMMERCIAL LAW -- GENERAL REGULATORY PROVISIONS -- | |
UNFAIR SALES PRACTICES | |
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1 | This act would require retailers of glucose monitors to provide a free, point of sale |
2 | replacement for any broken or defective monitor within twenty-four (24) hours of the request. |
3 | This act would take effect on January 1, 2025. |
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LC005400 | |
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