MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2019-02-04 for COOK CERVICAL RIPENING BALLOON W/STYLET J-CRBS-184000 manufactured by Cook Inc.
[134901645]
(b)(6). Occupation: other healthcare professional. (b)(4). This report includes information known at this time. A follow up report will be submitted should additional relevant information become available.
Patient Sequence No: 1, Text Type: N, H10
[134901647]
It is reported that during an unblinded randomized clinical trial of methods for inducing labor, the patient had a cook cervical ripening balloon placed. After an unspecified time interval, the patient had a spontaneous vaginal delivery with a blood loss of 700ml following delivery. Approximately 2 hours later, the patient required surgical/manual removal of her placenta, and had an additional 1000ml of blood loss. The patient was given ergometrine 500mcg intramuscularly, syntometrine 2 ml intramuscularly, and syntocinon 40iu intravenously to treat post-partum hemorrhage with resolution. In addition, the patient was given the antibiotics cefuroxime 1. 5 gm intravenously, and metronidazole 500mg intravenously prophylactically due to surgical intervention. The physician stated that there is no causal relationship between the cook cervical ripening balloon and the events reported. Additional information has been requested regarding the patient and the event. At the time of this report, no further information has been provided.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1820334-2019-00293 |
| MDR Report Key | 8302058 |
| Report Source | FOREIGN,HEALTH PROFESSIONAL,O |
| Date Received | 2019-02-04 |
| Date of Report | 2019-02-28 |
| Date of Event | 2018-03-19 |
| Date Mfgr Received | 2019-02-13 |
| Date Added to Maude | 2019-02-04 |
| 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. LARRY POOL |
| Manufacturer Street | 750 DANIELS WAY |
| Manufacturer City | BLOOMINGTON IN 47404 |
| Manufacturer Country | US |
| Manufacturer Postal | 47404 |
| Manufacturer Phone | 8123392235 |
| Manufacturer G1 | COOK INC |
| Manufacturer Street | 750 DANIELS WAY |
| Manufacturer City | BLOOMINGTON IN 47404 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 47404 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | COOK CERVICAL RIPENING BALLOON W/STYLET |
| Generic Name | PFJ, DILATOR, CERVICAL, HYGROSCOPIC-IAMINARIA |
| Product Code | PFJ |
| Date Received | 2019-02-04 |
| Catalog Number | J-CRBS-184000 |
| Lot Number | UNKNOWN |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COOK INC |
| Manufacturer Address | 750 DANIELS WAY BLOOMINGTON IN 47404 US 47404 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Other | 2019-02-04 |