Returns and Recalls Sample Clauses

Returns and Recalls. Each Party shall immediately provide the other Parties with notification of any event or occurrence that could necessitate the need to recall or withdraw Product(s) together with such information as may be available concerning the potential need to withdraw or recall Product(s). In the event of such event or occurrence concerns a failure to Produce Products in conformance with the Standards, Seller may request the return of any such Products in the possession of Juice Plus+. Juice Plus+ shall manage all recall decisions with respect to Products sold or shipped by Juice Plus+ which do not involve a claim of failure of the Products to be Produced in accordance with the Standards. In the event of any action described in this Section 32 that does involve a claim the Products were not Produced in accordance with the Standards, the Parties shall cooperate in determining, and will mutually agree upon, the response, if any, to be made to such action and each party agrees to cooperate with the other in responding to any communication or inquiry and/or attempting to resolve any such action.

Returns and Recalls. Seller shall immediately provide NSA with notification of any event or occurrence that could necessitate the need to recall or withdraw Products together with such information as may be available to Seller concerning the degree to which the reasons may have application to any Products shipped to or on behalf of NSA. In the event of such event or occurrence, Seller may request the return of any such Products in the possession of NSA or its Master Distributors. NSA shall manage all recall decisions with respect to Products sold or shipped by it to its Master Distributors and/or customers.

Returns and Recalls. If at any time any Buyer believes that its finished goods should be recalled and/or be the subject of a notification to a governmental authority because any of the relevant Products shall have failed to meet its Specifications or was otherwise noncompliant, such Buyer shall promptly notify Novopharm in writing of such belief and provide to Novopharm all information it has received in connection therewith. If at any time Novopharm believes that any finished goods should be recalled and/or be the subject of a notification to a governmental authority because the relevant Products shall have failed to meet Specifications or were otherwise noncompliant, Novopharm shall promptly notify the appropriate Buyer in writing of such belief and provide to such Buyer all information it has received in connection therewith. The appropriate Buyer shall, at Novopharm's sole cost and expense, be responsible for conducting any recall that is initiated and for complying with any and all regulatory requirements applicable to any such recall. Novopharm shall assist such Buyer by providing information reasonably needed by such Buyer to conduct such recall and to comply with regulatory requirements.

Returns and Recalls. 4.1 If at any time Vita Health believes that its finished goods should be recalled and/or be the subject of a notification to a governmental authority because any of the relevant Products will have failed to meet its Specifications or was otherwise noncompliant, Vita Health will promptly notify the applicable Buyer in writing of such belief and provide to the applicable Buyer all information it has received in connection therewith. If at any time a Buyer believes that any finished goods should be recalled and/or be the subject of a notification to a governmental authority because the relevant Products will have failed to meet Specifications or were otherwise noncompliant, the Buyer will promptly notify Vita Health in writing of such belief and provide to Vita Health all information it has received in connection therewith. The applicable Buyer will, at Vita Health's sole cost and expense, be responsible for conducting any recall that is initiated and for complying with any and all regulatory requirements applicable to any such recall. Vita Health will assist such Buyer by providing information reasonably needed by such Buyer to conduct such recall and to comply with regulatory requirements.

Returns and Recalls. CORD shall assist in the processing of Product returns, including recall returns. The fees to be paid to CORD for these return services are described in Section 8. CORD shall process Customer Product return authorizations and credits as set forth in the Operating Guidelines ("Product Return Services"). The fee for such Product Return Services by CORD will be included as a part of the Customer Service Fees described in Section 8. If Client is required to recall, or, on its own initiative, recalls any Product, CORD will assist Client with that recall in all ways reasonably requested by Client ("Product Recall Services"); provided that Client shall pay to CORD an amount equal to all reasonable costs incurred by CORD in connection with any such Product Recall Services..

Returns and Recalls. CORD shall accept and process Product returns, including recall returns, pursuant to this agreement and any applicable Operating Guidelines. The fees to be paid to CORD for these return services are described inss.8 of this agreement. Under normal operating conditions, CORD shall process all Customer return requests which comply with the terms of this agreement (including any applicable Operating Guidelines) within 5 business days following receipt of the returned Products and dispose of the returned Products as required by this agreement and applicable law. In addition, CORD shall assist Orphan in all ways reasonably requested by Orphan with respect to the processing of customer complaints relating to any returned Products or the handling of those returned Products. If Orphan is required to recall, or, on its own initiative, recalls any Products, CORD will assist Orphan with that recall in all ways reasonably requested by Orphan; provided that Orphan shall pay to CORD an amount equal to all costs incurred by CORD in connection with any such recall.

Returns and Recalls. Any Products that are: damaged during shipment, incorrectly shipped (including overage and/or incorrect Products/SKU), defective, dangerous, incomplete, infringing upon any third party intellectual property rights, not in compliance with applicable laws and regulations, or otherwise do not comply with iHerb policies and procedures will be replaced and reshipped, at Vendor’s expense, in accordance with iHerb’s Supplier Manual. In the event of any and all recalls of Products that are either (i) agreed to by Vendor or iHerb, or (ii) that are required either by law or in the commercially reasonable judgement of iHerb (because iHerb has reason to believe that Products are defective, dangerous, incomplete, infringe upon intellectual property rights, or are not in compliance with applicable laws or regulations), the Products will be returned to Vendor at Vendor’s expense as outlined in iHerb’s Supplier Manual. Upon Vendor’s knowledge of a recall, Vendor shall immediately notify iHerb. iHerb will ensure that all Products recalls are immediately communicated with applicable iHerb customers upon receipt of Vendor’s notice.

Returns and Recalls. ‌ 6.1 All sales are final with no Product return. 6.2 Where there is a requirement under applicable Law, GMP or GDP to order a Product recall (“Requirement to Recall”) in the Territory in respect of the Product, the Supplier shall be responsible for making any Product recall decisions in respect of such recall, and for initiating and executing any such Product recall in accordance with applicable Law. Without limiting the generality of the foregoing, the Supplier shall: 6.2.1 promptly (taking into consideration the potential impact of the continued use of the Product on patients, service users and the Authority as well as compliance by the Supplier with applicable Law, including any regulatory requirements) notify the Authority in writing of the recall together with the circumstances giving rise to the recall;‌ 6.2.2 from the date of the Requirement to Recall, where it is agreed between the Parties after the conduct of further investigation (to be completed within ten (10) Business Days of notifying the Authority pursuant to paragraph 6.2.1 of this Appendix 2), or determined in accordance with paragraph 5.4 and 5.6 of this Appendix 2 that the Requirement to Recall was caused by Defective Product as at the time of Delivery, treat the Product that is the subject of such recall as Defective Product in accordance with paragraph 5.4 of this Appendix 2, or, where arising in respect of Distribution section 3.4 of this Agreement shall apply; 6.2.3 consult with the Authority as to the most efficient method of executing the recall of the Product and use its Commercially Reasonable Efforts to minimise the impact on the Authority of the recall in accordance with the following: (a) If the Requirement to Recall is due to noncompliance with GMP or GDP, or in respect of the manufacturing, storage (except to the extent such storage is by the Authority), Delivery or Distribution of the Product, the recall shall be carried out wholly at the cost of the Supplier; (b) If the Requirement to Recall relates to any other issues other than those set out in (a), the recall shall be wholly at the cost of the Authority. Distribution sites: Those pharmacy departments within NHS hospitals within Great Britain, or in the case of Distribution to Northern Ireland, which shall apply only where such Product for Northern Ireland is supplied under a 174A Approval, the NHS central warehouse in Belfast, Northern Ireland. For the avoidance of doubt this shall not include any sites within:(i) the U...

Returns and Recalls