MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2018-06-19 for PENCAN N/A 4502051-13 manufactured by B. Braun Melsungen Ag.
[111917204]
(b)(6) this report has been identified as b. Braun (b)(6) (b)(4) internal report # 400391457 at this time, the device was not yet returned for evaluation. A follow-up report will be provided after the inspection results are available.
Patient Sequence No: 1, Text Type: N, H10
[111917205]
(b)(4). Broken needle.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9610825-2018-00109 |
| MDR Report Key | 7614842 |
| Report Source | FOREIGN,HEALTH PROFESSIONAL |
| Date Received | 2018-06-19 |
| Date of Report | 2018-08-30 |
| Date of Event | 2018-04-27 |
| Date Facility Aware | 2018-06-18 |
| Report Date | 2018-08-30 |
| Date Reported to FDA | 2018-08-30 |
| Date Reported to Mfgr | 2018-08-30 |
| Date Mfgr Received | 2018-06-04 |
| Device Manufacturer Date | 2017-08-07 |
| Date Added to Maude | 2018-06-19 |
| 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 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. JONATHAN SEVERINO |
| Manufacturer Street | 901 MARCON BLVD. |
| Manufacturer City | ALLENTOWN 18109 |
| Manufacturer Country | US |
| Manufacturer Postal | 18109 |
| Manufacturer Phone | 4847197287 |
| Manufacturer G1 | B. BRAUN MELSUNGEN AG |
| Manufacturer Street | CARL-BRAUN-STR. 1 |
| Manufacturer City | MELSUNGEN, 34212 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 34212 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PENCAN |
| Generic Name | SPINAL NEEDLE |
| Product Code | MIA |
| Date Received | 2018-06-19 |
| Returned To Mfg | 2018-06-26 |
| Model Number | N/A |
| Catalog Number | 4502051-13 |
| Lot Number | 17H07H8B21 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | B. BRAUN MELSUNGEN AG |
| Manufacturer Address | CARL-BRAUN-STR. 1 MELSUNGEN, HESSEN 34212 GM 34212 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2018-06-19 |