FDA Adverse Event
Malfunction
Summary report: N
BUDDE HALO RETRACTOR
MDR report key: 3928502
·
Received June 9, 2014
Report
- Report Number
- 3004608878-2014-00089
- Event Type
- Malfunction
- Date Received
- June 9, 2014
- Report Date
- May 15, 2014
- Manufacturer
- INTEGRA LIFESCIENCES CORPORATION OH/USA
- Product Code
- GZT
- PMA / PMN Number
- K830332
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
TO DATE, THE DEVICE INVOLVED IN THE REPORTED INCIDENT HAS NOT BEEN RECEIVED FOR EVALUATION. AN INVESTIGATION HAS BEEN INITIATED BASED UPON THE REPORTED INFORMATION.
Description of Event or Problem · 1
AN A1040 WAS FOUND TO BE DEFECTIVE UPON INCOMING INSPECTION. THE EVENT WAS DESCRIBED AS; COMPONENT NUMBER 438B1011 WAS FOUND TO HAVE A HOLE AT A RAIL SLIDING PORTION OF THE UNIT. THERE WAS NO PATIENT CONTACT REPORTED WITH THIS COMPLAINT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 334600 | BUDDE HALO RETRACTOR | RETRACTOR SYSTEMS | GZT | INTEGRA LIFESCIENCES CORPORATION OH/USA | 137 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |