MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,07 report with the FDA on 2012-08-13 for MICRO-PACE 4570 manufactured by Pace Medical, Inc..
[2860952]
Pace medical was notified on april 28, 2011 by (b)(6) via leter that unit had a fault.
Patient Sequence No: 1, Text Type: D, B5
[10127188]
Customer returned device with the complaint that there was no ventricular output. Upon examination of the device, it was confirmed there was no ventricular output. A component was re-soldered. The pacemaker was re-calibrated and final tested. All tests were normal and the device was returned to the customer. Reason for complaint: a failure of a solder joint. This may have been caused by rough handling or sudden impact.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 1218087-2012-00023 |
| MDR Report Key | 2699045 |
| Report Source | 01,07 |
| Date Received | 2012-08-13 |
| Date Mfgr Received | 2011-05-10 |
| Device Manufacturer Date | 2005-06-01 |
| Date Added to Maude | 2012-08-24 |
| 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 | BIOMEDICAL ENGINEER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Street | 310 SOUTH STREET SUITE2 |
| Manufacturer City | PLAINVILLE MA 02762 |
| Manufacturer Country | US |
| Manufacturer Postal | 02762 |
| Manufacturer Phone | 5083163861 |
| Single Use | 3 |
| Remedial Action | RP |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | MICRO-PACE |
| Generic Name | TEMPORARY CARDIAC PACEMAKER |
| Product Code | JOQ |
| Date Received | 2012-08-13 |
| Returned To Mfg | 2011-04-28 |
| Model Number | 4570 |
| Catalog Number | 4570 |
| Lot Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | PACE MEDICAL, INC. |
| Manufacturer Address | PLAINVILLE MA 02762 US 02762 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2012-08-13 |