| Model Number |
G52251 |
| Health Effect - Clinical Code |
No Known Impact Or Consequence To Patient (2692)
|
| Date of Event |
08/20/2015
|
|
Type of Reportable Event
|
Malfunction
|
|
Additional Manufacturer Narrative
|
|
This mdr is being filed after the associated complaint was reviewed under remediation protocol (b)(4), complaint/mdr retrospective review and remediation and reassessed as reportable.Additional complaint investigation and record remediation was not performed.
|
| |
|
Event or Problem Description
|
|
During a procedure, the balloon burst at 8atm.No part of the device was left in the patient's body, and no injuries or additional medical intervention occurred.
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Search Alerts/Recalls
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