FDA Adverse Event
Injury
Summary report: N
CRAWFORD
MDR report key: 284453
·
Received June 30, 2000
Report
- Report Number
- 284453
- Event Type
- Injury
- Date Received
- June 30, 2000
- Date of Event
- June 23, 2000
- Report Date
- June 27, 2000
- Manufacturer
- WALSH MANUFACTURING LTD.
- Product Code
- HNW
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- IL, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
THIS IS A PT WHO UNDERWENT A DACRYOCYSTORHINOSTOMY ON THE RIGHT SIDE. A LACRIMAL INTUBATION SET WAS USED AND ABOUT HALF OF THE WIRE BROKE OFF AND REMAINED IN THE PT'S NOSTRIL. THE PT WILL RETURN TO SURGERY IN 10 DAYS FOR REMOVAL OF FOREIGN BODY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CRAWFORD | LACRIMAL INTUBATION SET | HNW | WALSH MANUFACTURING LTD. | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 88 YR | Required Intervention |