Common use of Product Recalls Clause in Contracts

Product Recalls. (a) In the event: (i) any Regulatory Authority or other national government authority issues a request, directive or order that the Product be recalled; (ii) a court of competent jurisdiction orders such a recall, or (iii) Theravance or Hospira reasonably determines that Product should be recalled, the parties shall take all appropriate corrective actions, and shall cooperate in any governmental investigations surrounding the recall.

Product Recalls. In the event that (a) In the event: (i) any Regulatory Authority or other national government authority issues a request, directive or order that the a Product be recalled; , (iib) a court of competent jurisdiction orders such a recall, or (iiic) Theravance Supplier or Hospira Buyer shall reasonably determines determine that a Product should be recalled, the parties Parties shall take all appropriate corrective actions, and shall cooperate in any governmental the investigations surrounding the recall.

Product Recalls. (a) In the event: event (i) any Regulatory Authority or other national government authority issues a request, directive or order that the Finished Product be recalled; (ii) a court of competent jurisdiction orders such a recall, or (iii) Theravance Orchid or Hospira reasonably determines that Finished Product should be recalled, the parties Parties shall take all appropriate corrective actions, and shall cooperate in any governmental investigations surrounding the recallrecall in accordance with the procedures set forth in the Technical/Quality Agreement.

Product Recalls. (a) In the event: event (i) any Regulatory Authority or other national government authority issues a request, directive or order that the Product be recalled; (ii) a court of competent jurisdiction orders such a recall, or (iii) Theravance or Hospira Revance reasonably determines that Product should be recalled, the parties shall take all appropriate corrective actions, and shall cooperate in any governmental investigations surrounding the recall.

Product Recalls. (a) In the event: (i) any Regulatory Authority or other national government authority issues a request, directive or order that the Product be recalled; (ii) a court of competent jurisdiction orders such a recall, ; or (iii) Theravance Kythera or Hospira reasonably determines that Product should be recalled, the parties shall take all appropriate corrective actions, and shall cooperate in any governmental investigations surrounding the recall.