MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,07 report with the FDA on 2015-07-28 for HL-20 TWIN PUMP manufactured by Maquet Cardiopulmonary Ag.
[6639092]
On (b)(6) 2013 it was reported by the (b)(4) at maquet medical (b)(4) through the msupport system complaint number (b)(4) that the tpm 20-330 twin roller pump module serial number (b)(4) displayed a beltslip error when running at 250 rpm but the display indicated 119 rpm. The rpm was measured with an external tachometer and it indicated 119 rpm.
Patient Sequence No: 1, Text Type: D, B5
[14217660]
Maquet medical system, usa submits this report on behalf of the legal manufacturer of the device maquet cardiopulmonary (b)(4). The device was evaluated by a (b)(4) technician and the optical tacho board, motor belt and belt pulley were replaced and the issue was resolved. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
Report Number | 8010762-2014-00914 |
MDR Report Key | 4944784 |
Report Source | 01,07 |
Date Received | 2015-07-28 |
Date of Report | 2013-09-05 |
Date of Event | 2013-09-05 |
Date Facility Aware | 2013-09-05 |
Report Date | 2013-09-05 |
Date Reported to Mfgr | 2013-09-05 |
Date Mfgr Received | 2013-09-05 |
Date Added to Maude | 2015-07-28 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | TINA EVANCHO |
Manufacturer Street | 45 BARBOUR POND DRIVE |
Manufacturer City | WAYNE NJ 07470 |
Manufacturer Country | US |
Manufacturer Postal | 07470 |
Manufacturer Phone | 9737097265 |
Manufacturer G1 | MAQUET CARDIOPULMONARY AG |
Manufacturer Street | KEHLER STRASSE 31 |
Manufacturer City | RASTATT, 76437 |
Manufacturer Country | GM |
Manufacturer Postal Code | 76437 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HL-20 TWIN PUMP |
Generic Name | FLOWMETER, BLOOD, CARDIOVASCULAR |
Product Code | DPW |
Date Received | 2015-07-28 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MAQUET CARDIOPULMONARY AG |
Manufacturer Address | KEHLER STRASSE 31 RASTATT, 76437 GM 76437 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-07-28 |