Catalog Number 004550003 |
Device Problems
Device Damaged Prior to Use (2284); Detachment of Device or Device Component (2907)
|
Patient Problems
No Consequences Or Impact To Patient (2199); No Patient Involvement (2645)
|
Event Date 08/17/2015 |
Event Type
malfunction
|
Manufacturer Narrative
|
(b)(4).The device sample was not returned for evaluation at the time of this report.
|
|
Event Description
|
The customer alleges that the plastic heel of the device fell off the blade in the packaging.
|
|
Manufacturer Narrative
|
(b)(4).The sample was not returned for evaluation; therefore, the complaint could not be confirmed.If the sample is returned, a follow-up report will be submitted with investigation results.
|
|
Event Description
|
The customer alleges that the plastic heel of the device fell off the blade in the packaging.
|
|
Search Alerts/Recalls
|