MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2009-10-21 for HOLTER 2010 PLUS SOFTWARE M3741A manufactured by Philips Medical Systems.
[1242798]
Philips determined that a waveform file was misidentified. This patient data mismatch did not lead to misdiagnosis.
Patient Sequence No: 1, Text Type: D, B5
[8421130]
Philips determined that a waveform file was misidentified. This patient data mismatch did not lead to misdiagnosis. The complaint is still being investigated. A follow-up report will be submitted upon completion of the investigation.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1218950-2009-01521 |
MDR Report Key | 1514545 |
Report Source | 05,06,07 |
Date Received | 2009-10-21 |
Date of Report | 2009-08-24 |
Date Mfgr Received | 2009-07-24 |
Device Manufacturer Date | 2009-03-01 |
Date Added to Maude | 2009-10-29 |
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 |
Health Professional | 0 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | PATTI NILL |
Manufacturer Street | 3000 MINUTEMAN RD. |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal | 01810 |
Manufacturer Phone | 9786593769 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HOLTER 2010 PLUS SOFTWARE |
Product Code | MLO |
Date Received | 2009-10-21 |
Model Number | M3741A |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PHILIPS MEDICAL SYSTEMS |
Manufacturer Address | 3000 MINUTEMAN RD. ANDOVER MA 01810 US 01810 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2009-10-21 |