FDA Adverse Event
Injury
Summary report: N
MALLINCKRODT
MDR report key: 1821450
·
Received August 25, 2010
Report
- Report Number
- 2936999-2010-01129
- Event Type
- Injury
- Date Received
- August 25, 2010
- Date of Event
- July 26, 2010
- Report Date
- July 27, 2010
- Manufacturer
- COVIDIEN, FORMERLY TYCO HEALTHCARE
- Product Code
- BTR
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
(B)(4). APPLICABLE 501K# FOR U.S. DISTRIBUTED PART IS K871204. THE SAMPLE ASSOCIATED TO THIS REPORT IS CURRENTLY IN TRANSIT TO THE MFG SITE FOR ANALYSIS. IF SIGNIFICANT INFO IS IDENTIFIED FROM THE INVESTIGATION, A SUMMARY OF THE INVESTIGATION RESULTS WILL BE PROVIDED IN A SUPPLEMENTAL REPORT.
Description of Event or Problem · 1
THE COMPANY RECEIVED A REPORT WHERE IT WAS CLAIMED THAT THE TUBE DEVELOPED A LEAK DURING PT USE. THE SOURCE OF THE LEAK COULD NOT BE IDENTIFIED. EXTUBATION AND REINTUBATION OF A REPLACEMENT TUBE WAS REQUIRED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MALLINCKRODT | 7.5MM LO CONTOUR MURPHY 86083 X10 | BTR | COVIDIEN, FORMERLY TYCO HEALTHCARE |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |