FDA Adverse Event
Malfunction
Summary report: N
SAPPHIRE M.T INFUSION PUMP- US
MDR report key: 14277033
·
Received May 4, 2022
Report
- Report Number
- 3010293992-2022-00007
- Event Type
- Malfunction
- Date Received
- May 4, 2022
- Date of Event
- March 31, 2022
- Report Date
- July 19, 2022
- Manufacturer
- EITAN MEDICAL LTD.
- Product Code
- FRN
- UDI-DI
- 07290109150109
- PMA / PMN Number
- K161667
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MI, US
- Reporter Occupation
- 501
Narratives
Additional Manufacturer Narrative · 0
EITAN MEDICAL LTD IS FORMERLY NAMED Q CORE MEDICAL LTD. THE FEI NUMBER IS THE SAME 3010293992.
Additional Manufacturer Narrative · 0
EITAN MEDICAL LTD IS FORMERLY NAMED Q CORE MEDICAL LTD. THE FEI NUMBER IS THE SAME (B)(4).
Description of Event or Problem · 0
THE COMPLAINT WAS REPORTED BY A CUSTOMER FROM USA: DELIVERY ISSUE.
Description of Event or Problem · 0
THE COMPLAINT WAS REPORTED BY A CUSTOMER FROM USA. LEAKAGE ISSUE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1243627 | SAPPHIRE M.T INFUSION PUMP- US | INFUSION PUMP | FRN | EITAN MEDICAL LTD. | 07290109150109 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown |