Autopen Classic Automatic insulin delivery pen, 3.0ml x 2 unit 2-42 units, AN3800, Lot 7JH, NDC 08470-3800-01, The product is a non-sterile automatic subcutaneous injection device which delivers insulin.
- Company
- Owen Mumford Usa, Inc.
- Recall Initiated
- December 11, 2014
- Posted
- July 15, 2015
- Terminated
- July 11, 2017
- Recall Number
- Z-2082-2015
- Quantity
- 225 units
- Firm Location
- Marietta, GA
Reason for Recall
The dials in the Autopens are not working - the dial does not stay dialed, but springs right back to 0. As a result, the patient could not dial up a dose of medicine to deliver via an injection.
Distribution
Nationwide Distribution including FL, IL, NV, NJ, OH, and TN.
Lot / Code Info
Lot 7JH, UPC Code 384703800014
Root Cause
Process control
Action Taken
Owen Mumford, Inc. sent an Urgent Medical Device Recall Notification letter dated December 19, 2014, to all affected customers via Fed Ex. The letter instructed customers to check their shelves for the product and specific lot number. The customer was instructed to contact Customer Service to obtain an RMA and a pre-paid, pre-addressed label for return of the devices. A form was included for the documentation of the inspection of their inventory, whether any are in stock and will be returned, and if they will provide a customer list of how they sold any devices to or that they will notify their customers of the issue with the product. They were instructed to fill it out and fax back to 770-977-2866. Customers with questions were instructed to contact Customer Service Department at 1-800-421-6936. For questions regarding this recall call 770-977-2226, ext 13.