Reformulated Products. For purposes of this Settlement Agreement, Reformulated Products are defined as Products containing DEHP in a maximum concentration of 1,000 parts per million (0.1%) when analyzed pursuant to U.S. Environmental Protection Agency testing methodologies 3580A and 8270C, or equivalent methodologies utilized by state or federal agencies for the purpose of determining DEHP content in a solid substance.
Reformulated Products. “Reformulated Products” are Products that: (a) contain no more than 90 parts per million (“ppm”) lead when analyzed pursuant to U.S. Environmental Protection Agency testing methodologies 3050B and 6010B or equivalent methodologies utilized by federal or state agencies for the purpose of determining lead content in a solid substance; and (b) yield no more than 1.0 microgram (“ug”) of lead when a wipe is applied to all surfaces according to NIOSH Test Method No. 9100.
Reformulated Products. Commencing on the Effective Date and continuing thereafter, Medline agrees that the Products it manufactures, imports, distributes, ships, sells or offers to ship for sale in California, will be “Reformulated Products.” For purposes of this Settlement, Reformulated Products comply with the following content limits: DEHP in concentration less than 1,000 parts per million (“ppm”) DEHP by weight in any Accessible Component (i.e. any component that may be touched or handled during a reasonably foreseeable use) when analyzed pursuant to EPA testing methodologies 3580A and 8270C, or equivalent methodologies utilized by state or federal agencies for the purpose of determining DEHP content in a solid substance.
Reformulated Products. Commencing ninety (90) days after the Effective Date, and continuing thereafter, all Products manufactured, imported, distributed, shipped, sold or offered for sale in California shall be “Reformulated Products.” For purposes of this Settlement Agreement, Reformulated Products are Products that: (a) contain no more than 90 parts per million (“ppm”) (0.09%) lead in any exterior decorations when analyzed pursuant to U.S. Environmental Protection Agency testing methodologies 3050B and 6010B or equivalent methodologies utilized by federal or state agencies for the purpose of determining lead content in a solid substance (e.g., ASTM C738-94 (2016)); (b) yield no more than 1.0 microgram (“μ g”) of lead when analyzed pursuant to NIOSH Test Method No. 9100 as applied to exterior decorations of the Product; and (c) a Reformulated Products shall yield a result of non-detect (defined as no more than 25 ppm (0.025%) by weight of lead) for any decorations located in the upper 20 millimeters of a Product, i.e., the “Lip-and-Rim” area of the vessel, or the decorative materials located on the interior surface of the Product (i.e., the beverage-containing portion) when analyzed pursuant to EPA testing methodologies 3050B and 6010B, or equivalent methodologies used by state and federal agencies to determine lead content in a solid substance (e.g., ASTM C927-80 (2014)).
Reformulated Products. Commencing on December 1, 2015, and continuing thereafter, Coda shall only purchase for sale or manufacture for sale in California, (a) “Reformulated Products”, or (b) Products that are sold with a clear and reasonable warning pursuant to Section 2.2, below. For purposes of this
Reformulated Products. Commencing on the Effective Date and continuing thereafter, Stansport shall only purchase for sale or manufacture for sale in California, Reformulated Products or Products that are sold with a clear and reasonable warning pursuant to Section 2.2. For purposes of this Settlement Agreement, “Reformulated Products” are Covered Products that contain no more than 1,000 parts per million (0.1%) DEHP content when analyzed pursuant to EPA testing methodologies 3580A and 8270C, or equivalent methodologies used by state or federal agencies for purposes of determining DEHP content in a solid substance. .
Reformulated Products. Commencing on the Effective Date, and continuing thereafter, all Products manufactured, imported, distributed, shipped, sold or offered for sale in California shall be “Reformulated Products.” For purposes of this Settlement Agreement, Reformulated Products are Products that: (a) contain no more than to 100 parts per million (“ppm”) lead when analyzed pursuant to U.S. Environmental Protection Agency testing methodologies 3050B and 6010B or equivalent methodologies utilized by federal or state agencies for the purpose of determining lead content in a solid substance; and (b) yield no more than 1.0 microgram (“ug”) of lead when a wipe is applied to all surfaces according to NIOSH Test Method No. 9100.
Reformulated Products. For purposes of this Consent Judgment, “Reformulated Products” are defined as Products containing a maximum concentration of 0.1 percent (1,000 parts per million) of each DEHP and Diisononyl phthalate (“DINP”) when sampled and analyzed pursuant to U.S. Environmental Protection Agency testing methodologies 3580A and 8270C, or other methodologies utilized by state or federal agencies for the purpose of determining DEHP and/or DINP content in a solid substance.
Reformulated Products. “Reformulated Products” are defined as those Products that: (a) contain no more than 90 parts per million (“ppm”) lead in any decoration, colored artwork, designs and/or marking on the surface of the Products when analyzed pursuant to U.S. Environmental Protection Agency testing methodologies 3050B or equivalent methodologies utilized by federal or state agencies for the purpose of determining lead content in a solid substance; and (b) yield no more than 1.0 microgram of lead on any surface sampled and analyzed pursuant to the NIOSH 9100 testing protocol or equivalent methodologies used by state and federal agencies to determine lead content on a solid substance. If the decoration is tested after it is affixed to the Product, the percentage of the lead by weight must relate only to the decorating materials and must not include any quantity attributable to non-decorating material (e.g., ceramic substrate).
Reformulated Products. The Covered Products shall be deemed to comply with Proposition 65 with regard to lead and be exempt from any Proposition 65 warning requirements for lead if the level of lead in the Covered Products is below 65 parts per billion, as determined by the average (arithmetic mean) of up to 3 results from laboratory analysis of the same lot of the Covered Products. Covered Products that were supplied or contracted to be supplied to third parties by Riverside prior to 6 months after the Compliance Date shall be deemed exempted from the requirements of this Section 2 and shall be permitted to be sold through as previously manufactured, packaged and labeled. Analyses must utilize a method that employs ICP-MS. Laboratories must have the capability of controlling lead contamination throughout the analytical process, including sample compositing, sample digestion, and the lead determination steps. In order to meet the analytical objectives, the use of high purity acids will be required as well the use of closed-vessel type sample digestion procedures. The conditions and procedures needed to successfully meet the analyses must comply with in the FDA Elemental Analysis Manual found here: • xxxx://xxx.xxx.xxx/Food/FoodScienceResearch/LaboratoryMethods/ucm2006954.htm • xxxx://xxx.xxx.xxx/downloads/Food/FoodScienceResearch/LaboratoryMethods/UCM37700 5.pdf Particular attention must be given to recovery information offered to attribute accuracy to these analyses. The levels of lead used to fortify products and ingredients for analyte recovery must be in the range of 50-200% of the lead level found in the product, if the level of lead in the product is in a quantifiable range. As a measure of accuracy, laboratories are also encouraged to provide recovery information on certified reference materials with lead levels similar to these products or ingredients. Participating laboratories must be accredited, preferably under ISO 17025 to conduct low level lead analyses in foods by ICP-MS. The analytical objective for lead analysis, i.e., the Limit of Quantification (LOQ), for finished products and for the major ingredients is 0.010 mg/kg.
