Medivators Endo carry-on Procedure Kit REF CPK-100222-0002 - Product Usage: is intended to be used with an air or CO2 source and/or a pump along with a sterile water source to supply air or CO2 and sterile water to an endoscope during endoscopic procedures.
Recall
- Recall Number
- Z-1778-2020
- Event Number
- 84109
- Firm
- Medivators, Inc.
- FEI Number
- 2150060
- Product Code
- FAJ
- Status
- Terminated
- Root Cause
- Equipment maintenance
- Initiated
- October 9, 2019
- Terminated
- December 11, 2020
- Address
- 14605 28th Ave N, Plymouth, MN, 55447-4822
Description
Medivators Endo carry-on Procedure Kit REF CPK-100222-0002 - Product Usage: is intended to be used with an air or CO2 source and/or a pump along with a sterile water source to supply air or CO2 and sterile water to an endoscope during endoscopic procedures.
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.
An Urgent Medical Device Recall Notification letter was sent to customers via certified mail next day delivery on 10/09/2019. The letter identified affected product, stated reason for recall, asked for product to be quarantined and discontinue use. Customers are to return product to Medivators by obtaining a Return Material Authorization from Customer Service. A response form was asked to be returned. Questions can be directed to Customer Service at 1-800-444-4729.
Worldwide distribution - US Nationwide distribution and the countries of Australia, England.
53,790 units total