SB 1102 Oklahoma Senate · 2026 Regular Session

Vapor products; modifying and adding requirements for certain attestation; requiring certain notice and directing seizure of certain products. Emergency.

SB 1102 modifies deadlines for vapor product regulations, moving key dates from September 1, 2026, to September 1, 2025. It requires vapor product sellers to provide updated certification (attestation) and mandates specific notice before product seizures. The bill directly affects manufacturers and retailers of vapor products in Oklahoma, imposing stricter compliance timelines. As an emergency measure, it accelerates existing regulatory requirements without adding new substantive provisions. The bill passed committee with a "Do Pass" recommendation and is now moving to the House.
Bill status passed 3 of 5 stages cleared
Introduction
Feb 2025
Committee Review
Apr 2025
Senate Passage
Mar 2025
House Passage
Governor
Introduced Feb 3, 2025 Last action Apr 9, 2025
Maddy AI version diff · 4 comparisons

What changed between versions

SB1102 (3-11-25) (COLEMAN) FA1.PDF Floor (Senate) · 5 edits
MODERATE
The bill was updated to shift key compliance deadlines from 2026 to 2025, likely to align with new fiscal or regulatory cycles. The text was reorganized to clearly define 'vapor products' and establish a mandatory annual attestation process for manufacturers, requiring them to certify FDA approval status and pay specific fees to the Attorney General. These changes aim to tighten oversight of vapor products by creating a clear, enforceable reporting mechanism with financial penalties for non-compliance.
Scope change
The scope of applicability remains focused on vapor product manufacturers selling in Oklahoma, but the specific dates for compliance and the structure of the reporting requirements have been significantly altered.
TIMELINE

Critical compliance deadlines were moved forward from September 1, 2026, to September 1, 2025, in multiple sections of the bill.

REQUIREMENT

A new mandatory annual attestation process was established, requiring manufacturers to submit sworn statements to the Attorney General certifying their product's FDA status.

FISCAL

New fees were introduced for the attestation process: a $5,000 initial fee and a $2,500 annual renewal fee for each manufacturer.

DEFINITION

Clear definitions were added for 'vapor product' and 'timely filed premarket tobacco product application' to clarify which items are subject to the new rules.

TECHNICAL

The document structure was changed from a committee amendment format to a formal Senate Floor version, incorporating bolded text to denote specific committee amendments.

Floor votes · Senate Mar 27, 2025

How they voted

3810
Passed · 1 other
Total votes 49
Mar 27, 2025
D Democratic9
8 Yea 1 Nay
88% Yea
R Republican40
30 Yea 9 Nay 1
75% Yea
Vote distribution
All Yea All Nay Mixed No data
Full legislative history

Actions timeline

Total actions
15
Key actions
4
Committee
4
Amendments
1
Apr 9, 2025
Lower · Passed
Policy recommendation to the Health and Human Services Oversight committee; Do Pass Alcohol, Tobacco and Controlled Substances
lower
Apr 1, 2025
Committee
Referred to Alcohol, Tobacco and Controlled Substances
lower
Mar 31, 2025
Introduced
First Reading
lower
Mar 31, 2025
Upper · Passed
Engrossed to House
upper
Mar 27, 2025
Committee
Referred for engrossment
upper
Mar 27, 2025
Upper · Passed
Measure and Emergency passed: Ayes: 37 Nays: 9
upper
Mar 27, 2025
Introduced
General Order, Amended
upper
Feb 27, 2025
Upper · Passed
Reported Do Pass Business and Insurance committee; CR filed
upper
Feb 3, 2025
Introduced
First Reading
upper
2 primary · 0 co-sponsors

Sponsors