It was reported a multiple joint silicone mcp procedure was performed on (b)(6) 2014.During billing it was discovered one of the implanted devices had expired.The distributor immediately informed the customer that an expired device had been used.The customer that an expired device had been used.The customer responded that they were aware of this.The distributor followed up with a member of the care team on (b)(6) 2014, and was told they were aware of the expired product being used.They noticed it after the patient had already left.At this time they are watching the patient for any adverse reactions and will take necessary medical actions if that occurs.The distributor reported to the manufacturer, for now the customer is aware of the issue and they are handling the issue internally.There is no complaint from the customer, no injury is alleged.
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