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The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Following its return to the local Arjo office and the availability of the permanent solution, a customer will be contacted to complete the action.ĭistribution in US - AZ, CA, CO, IL, LA, MA, MI, MO, OH, PA, WAġ A record in this database is created when a firm initiates a correction or removal action. The Field Safety Notice will be accompanied by Customer Response Form. Contact Arjo to ask to an Arjo service technician to visit a customer facility to perform the scale disconnection to continue to use the ceiling lift safely. Contact Arjo to order parts and instruction required to proceed with the disconnection of the affected scale by on-site biomed personnel to continue to use the ceiling lift safely, or The spreader bar can disconnect from the scale bottom attachment.Ĭustomers identified as owners of the affected scales will be notified of the identified product risk and the Field Safety Corrective Action through the Field Safety Notice.Īffected customers need to ensure that all caregivers and users of the affected devices are made aware of the Field Safety Notice. Maxi Sky 1000 (Arjo) and V10 (BHM) Bariatric Ceiling Rail - Mounted Lift with measuring functionĪll units of Model 700-00536: Class III 454 kg scale and Model 700-00526: 454 kg scale
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Product recall the office script code#
Lift, patient, non-ac-powered - Product Code FSA Class 2 Device Recall Maxi Sky 1000 (Arjo) and V10 (BHM)