FDA Adverse Event
Injury
Summary report: N
MP-28 SOFPORT PLACEMENT SYSTEM
MDR report key: 2923262
·
Received October 11, 2006
Report
- Report Number
- 1920664-2006-01440
- Event Type
- Injury
- Date Received
- October 11, 2006
- Date of Event
- September 1, 2006
- Report Date
- September 15, 2006
- Manufacturer
- BAUSCH & LOMB
- Product Code
- MSS
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TN, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
WHILE INSERTING THE LENS INTO THE PATIENT'S EYE, THE LENS DID NOT EXIT CORRECTLY IN THE DELIVERY DEVICE. THE LENS WAS REMOVED AND REPLACED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MP-28 SOFPORT PLACEMENT SYSTEM | INTRAOCULAR LENS | MSS | BAUSCH & LOMB | H610801 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |