MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2018-01-04 for PENCAN? 333851 manufactured by B. Braun Medical Inc..
[96340428]
(b)(4). The device involved has yet been received for evaluation and the investigation is ongoing at this time. A follow-up report will be submitted when the results of the investigation become available.
Patient Sequence No: 1, Text Type: N, H10
[96340429]
As reported by the user facility: during insertion of the needle, the end broke off and stayed in the patient. The patient was converted to general anesthesia for the c-section. After delivery an ultrasound was used to locate the retained needle and an x-ray was used to confirm the position. It was concluded during the spinal surgery consultation that at this time they will wait to remove the needle. The patient started a course of antibiotics and will follow up in a few weeks.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2523676-2017-00177 |
| MDR Report Key | 7163628 |
| Report Source | HEALTH PROFESSIONAL,USER FACI |
| Date Received | 2018-01-04 |
| Date of Report | 2018-01-04 |
| Date of Event | 2017-12-08 |
| Date Mfgr Received | 2017-12-08 |
| Device Manufacturer Date | 2017-10-18 |
| Date Added to Maude | 2018-01-04 |
| 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 | JONATHAN SEVERINO |
| Manufacturer Street | 901 MARCON BLVD |
| Manufacturer City | ALLENTOWN PA 18109 |
| Manufacturer Country | US |
| Manufacturer Postal | 18109 |
| Manufacturer Phone | 4847197287 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PENCAN? |
| Generic Name | SPINAL ANESTHESIA KIT |
| Product Code | OFU |
| Date Received | 2018-01-04 |
| Catalog Number | 333851 |
| Lot Number | 0061577133 |
| Device Expiration Date | 2019-05-31 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | B. BRAUN MEDICAL INC. |
| Manufacturer Address | 901 MARCON BLVD ALLENTOWN PA 18109 US 18109 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2018-01-04 |