FDA Adverse Event
Malfunction
Summary report: N
MEDLINE
MDR report key: 1208864
·
Received October 21, 2008
Report
- Report Number
- MW5008714
- Event Type
- Malfunction
- Date Received
- October 21, 2008
- Report Date
- October 21, 2008
- Manufacturer
- MEDLINE IND.
- Product Code
- LRP
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- MS, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
RECEIVED DISPOSABLE SUTURE REMOVAL TRAYS WITH NOTICEABLE SUBSTANCE ADHERED TO THE INSTRUMENTS WITHIN THE STERILE PACK.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MEDLINE | SUTURE REMOVAL TRAY | LRP | MEDLINE IND. | 08DA0236 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |