Recall StatusTerminated
Date Initiated2017-02-14
Date Terminated2017-11-03
Product Quantity3232
Reason for Recall
Digital templates were created with the incorrect files.
Firm Action
On 2/14/2017 URGENT MEDICAL DEVICE CORRECTION notifications were sent to the affected users and 3rd party users via email. The recall notification included a description of the reason for the recall, affected product, consignee responsibilities, and instructions for 3rd party users to respond to the formal recall notification.
Orthosize Templating Users
In approximately 6 weeks you will receive a notice that an update is available for the Orthosize Templating App. Upon selecting the app you will be required to update the app in order to use it.
1. Review this notification and ensure affected personnel are aware its contents.
2. Immediately update the app when the update becomes available.
3. If after reviewing this notice you have further questions or concerns please call 411 Technical
Services at 574-371-3071 between 8:00 am and 5:00pm EST, Monday through Friday.
Alternatively, your
questions may be sent by email to
[email protected]
Digital Template Users (3rd party)
1. Review this notification and ensure affected personnel are aware of the contents.
2. Immediately update your systems to include the revised digital templates included with notice.
3. Complete Attachment 1 Certificate of Acknowledgement.
a. Return a digital copy to
[email protected].
b. Retain a copy of the Acknowledgement Form with your records.
4. If after reviewing this notice you have further questions or concerns please call 411 Technical
Services at 574-371-3071 between 8:00 am and 5:00pm EST, Monday through Friday. Calls
received outside of the call center operating hours will receive a prompt to record a voicemail or
be transferred to an on-call representative in the case of an emergency. Alternatively, your
questions may be sent by email to
[email protected]
Root Cause
Software Manufacturing/Software Deployment
Distribution Pattern
Worldwide distribution. US Nationwide including Puerto Rico, Canada, Argentina, Australia, Austria, Belgium, Chile, China, Denmark, Finland, France, Germany, Greece, India, Italy, Japan, Korea, Lithuania, Malaysia, Mexico, Netherlands, Nicaragua, Norway, Pakistan, Poland, Portugal, Romania, Singapore, South Africa, Spain, Sweden, Switzerland, Turkey, United Kingdom.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.