FDA Adverse Event
Malfunction
Summary report: N
MALLINCKRODT
MDR report key: 3912446
·
Received May 13, 2014
Report
- Report Number
- 2936999-2014-00414
- Event Type
- Malfunction
- Date Received
- May 13, 2014
- Date of Event
- April 1, 2014
- Report Date
- April 16, 2014
- Manufacturer
- COVIDIEN
- Product Code
- BTR
- PMA / PMN Number
- K090352
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- KN
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
(B)(4). THE SAMPLE ASSOCIATED TO THIS REPORT IS EXPECTED TO BE RETURNED FOR ANALYSIS. IF THE SAMPLE IS RECEIVED, A SUMMARY OF THE INVESTIGATION RESULTS WILL BE PROVIDED IN A SUPPLEMENTAL REPORT.
Description of Event or Problem · 1
CUSTOMER REPORTED, WHILE THE NURSE PROCESSED THE CUFF TEST, SHE FOUND THE AIR LEAKED FROM THE CUFF. CUSTOMER CONFIRMED THAT FAULT WAS IDENTIFIED DURING PRETESTING EFFORTS. NO PATIENT INVOLVEMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 285492 | MALLINCKRODT | TAPERGUARD ORAL/NASAL TRACHEAL TUBE | BTR | COVIDIEN | 13E0577JZX |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |