MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2018-01-05 for PENCAN? 333851 manufactured by B. Braun Medical Inc..
[96620050]
(b)(4). The device involved has not 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
[96620171]
As reported by user facility: during a spinal procedure, the introducer bent creating metal fragments. No known patient injury.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2523676-2017-00183 |
MDR Report Key | 7169088 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2018-01-05 |
Date of Report | 2018-01-05 |
Date of Event | 2017-12-11 |
Date Mfgr Received | 2017-12-12 |
Date Added to Maude | 2018-01-05 |
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 | 2018-01-05 |
Catalog Number | 333851 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
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 | 2018-01-05 |