U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
데이터 추가 비고
Drape, surgical - Product Code KKX
원인
The reason for the recall is that the inner carton box of the rolled probe cover pc0907nb has the incorrect expiration date (2015-10-01) on the label while the individual pouch labels and outer shipper have the correct expiration date (2018-10-01). the
manufacturing date was inadvertently used as the expiration date on the inner carton box labels.
조치
Ecolab sent an "Urgent Medical Device Recall" letter dated November 30, 2016, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.
Customers were advised to quarantine the product for return. If the product was further distributed notify them of the recall. Requested customers to complete and return the Recall Response Form.
For questions contact Customer Service by phone at 1-800-824-3027 or e-mail customerservice@microtekmed.com.
For further questions please call (651) 250-4385.