MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2020-03-24 for FETAL SPIRAL ELECTRODE 989803137631 manufactured by Philips Medical Systems.
[184708549]
Serial number unknown. A follow-up report will be submitted once the investigation is complete.
Patient Sequence No: 1, Text Type: N, H10
[184708550]
It was reported that the fetal scalp electrode became stuck in the fetal scalp requiring an incision to remove the electrode.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1218950-2020-01892 |
MDR Report Key | 9873497 |
Report Source | FOREIGN,USER FACILITY |
Date Received | 2020-03-24 |
Date of Report | 2020-03-20 |
Date of Event | 2020-02-12 |
Date Mfgr Received | 2020-03-20 |
Date Added to Maude | 2020-03-24 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. ROBERT CORNING |
Manufacturer Street | 3000 MINUTEMAN ROAD |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal | 01810 |
Manufacturer Phone | 9786871501 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | FETAL SPIRAL ELECTRODE |
Generic Name | FETAL SPIRAL ELECTRODE, SINGLE |
Product Code | HGP |
Date Received | 2020-03-24 |
Model Number | 989803137631 |
Catalog Number | 989803137631 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PHILIPS MEDICAL SYSTEMS |
Manufacturer Address | 3000 MINUTEMAN ROAD ANDOVER MA 01810 US 01810 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-24 |