FDA Adverse Event
Malfunction
Summary report: N
ANIMAS VIBE
MDR report key: 6679833
·
Received June 29, 2017
Report
- Report Number
- 2531779-2017-13629
- Event Type
- Malfunction
- Date Received
- June 29, 2017
- Report Date
- June 2, 2017
- Manufacturer
- ANIMAS CORPORATION
- Product Code
- OYC
- UDI-DI
- 10840406100228
- PMA / PMN Number
- P130007
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NC, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
DEVICE EVALUATION: THE PUMP HAS BEEN RETURNED AND EVALUATED BY PRODUCT ANALYSIS ON 6/02/2017 WITH THE FOLLOWING FINDINGS: DURING TESTING, THE PUMP POWERED ON WITH A LOW SOUND FUNCTION. (B)(6).
Description of Event or Problem · 1
THE PUMP WAS RETURNED FOR INVESTIGATION. INVESTIGATION REVEALED A LOW SOUND FUNCTION. THIS REPORT IS MADE BASED ON RESULTS OF INVESTIGATION COMPLETED ON 6/02/2017.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 460352 | ANIMAS VIBE | INSULIN INFUSION PUMP | OYC | ANIMAS CORPORATION | 10840406100228 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 86 YR |