Product Defect means a defect as referenced in the CPSA and defined in Commission regulations at 16 CFR 1115.4.
Product Defect means any defect in any Product including, without limitation, in the workmanship, in the manufacture of, in the ingredients or raw materials comprising or in the labeling or packaging of any Product.
Product Defect means the serious, pervasive, and dangerous design and manufacturing defects that render the WEN Hair Care Products unmerchantable and unsuitable for use and which place persons at risk of serious injury, including the presence of harmful chemicals which cause inter alia major hair loss, stunted hair growth, hair breakage, brittle, limp and/or lifeless hair, dermatitis, eczema, blistering, rash, scabbing, peeling, reddening and swelling, sore, tender, and/or irritated scalp, itchiness, redness, and other severe medical injuries;
Examples of Product Defect in a sentence
Any damages to a Product that is not installed by a Accredited Installer shall be deemed to be caused by the incorrect installation, subject to credible evidence provided by the End User that shows that the damages are indeed caused by a Product Defect.
The owner of the defected Product must notify Soltaro of a Product Defect within the defined warranty period (including any valid Warranty Extension).
Also, the Product Defect does not include any cosmetic changes or other changes in Q CELLS Product appearance, including but not limited to, any color changes, mold and normal wear and tear.
However, any Product Defect that would not be discoverable upon a reasonable inspection of a Product (a “Hidden Defect”) will not be deemed accepted by ETON at any time.
In the event that an Insured becomes aware of a Product Defect, the Insured shall locate and recall all relevant Products at its own expense, regardless whether or not Personal Injury or Property Damage has already occurred.
More Definitions of Product Defect
Product Defect is the root cause of loss of function, degradation of function or intermittent function performance.
Product Defect means a defect that causes a Product to not conform to the Specifications and/or to the Product Warranty.
Product Defect means “product defect” as used in 15 U.S.C.
Product Defect mean? What Is Excluded?
8.1 Normal wear and tear should not result in Product failure, and is not covered by this Warranty.
8.2 Using the Product in ways outside its normal or intended use may damage the Product, or cause later failure, and is not covered by this Warranty, Including but not limited to: Accidents Abuse Misuse Neglect
Product Defect means any Warranty Claim based exclusively on a product design defect, material defect, and/or workmanship defect in any particular product; and "Claim Threshold" shall mean four tenths of one (.4%) percent of the Buyer's revenue from the sale of the products identified on Schedule 2.
Product Defect means Drug Product not conforming to RTU's obligations for Drug Product pursuant to Article 2.1 and pursuant to batch testing and release and includes a Latent Defect.
Product Defect means Drug Product not conforming to RTU's obligations for Drug Product pursuant to Article 2.1 and pursuant to batch testing and release and includes a Latent Defect. Article 1.22. "Regulatory Approval" means any and all approvals, licenses (including product and establishment licenses), registrations, or authorizations of any Regulatory Authority necessary to develop, manufacture, commercialize, promote, distribute, transport, store, use, sell or market the Drug Substance or Drug Product for use in the SAG Territory. Article 1.23. "Regulatory Authority" means any national, supra-national, regional, federal, state, provincial or local regulatory agency, department, bureau, commission, council or other governmental entity regulating or otherwise exercising authority over the distribution, importation, exportation, manufacture, use, storage, transport, clinical testing or sale of the Drug Substance or Drug Product. Article 1.24. "Regulatory Filings" means, with respect to the Product in the Territory, all applications, registrations, licenses, authorizations and approvals (including all Regulatory Approvals), all correspondence submitted to or received from the Regulatory Authorities (including minutes and official contract reports relating to any communications with any Regulatory Authority) and all supporting documents, and all data contained in any of the foregoing. Article 1.25. "SKU(s)" means Stock Keeping Unit(s) in different product formats used as the smallest unit of measure to identify manufacturing and distribution of the Drug Product. Article 1.26. "Specifications" mean the manufacturing, formulation, quality control, packaging, labeling, shipping and storage specifications as separately set out for Drug Substance and Drug Product in Appendix B and as updated from time to time on mutual agreement in writing by the Parties. Article 1.27. "SAG Territory" means all of the countries that are located in North, Central and South America, including the Caribbean, and their territories and possessions; all of the countries located in Japan, Asia and Oceania, and their territories and possessions; and all of the countries located in EU, Middle East, Africa, and their territories and possessions; except Japan, United States and Canada so long as the SPL Agreement and the Supply Agreement respectively, have not been terminated. Article 1.28. "Term" means the definition set forth in Article 11.1. Article 1.29. "Third Parties" means any Person other than SAG...