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 2020-03-13 for WEBER MEDULLARY PLUG N/A UNKNOWN manufactured by Zimmer Gmbh.
[183277581]
The manufacturer did receive x-rays, or other source documents for review. The manufacturer did not receive the device for investigation. As no lot number was provided, the device history records could not be reviewed. A cause for this specific event cannot be ascertained from the information provided. As soon as supplemental information becomes available an updated report will be submitted. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[183277582]
A significant amount of cement has leaked past the plug.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 0009613350-2020-00117 |
MDR Report Key | 9828839 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2020-03-13 |
Date of Report | 2020-03-13 |
Date of Event | 2019-11-13 |
Date Mfgr Received | 2020-02-24 |
Date Added to Maude | 2020-03-13 |
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 | MS. CHRISTINA ARNT |
Manufacturer Street | 56 E. BELL DR. |
Manufacturer City | WARSAW IN 46582 |
Manufacturer Country | US |
Manufacturer Postal | 46582 |
Manufacturer Phone | 5745273773 |
Manufacturer G1 | ZIMMER GMBH |
Manufacturer Street | SULZER ALLEE 8 SULZER INDUSTRIE PARK |
Manufacturer City | WINTERTHUR 8404 |
Manufacturer Country | SZ |
Manufacturer Postal Code | 8404 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | N/A |
Event Type | 3 |
Type of Report | 3 |
Brand Name | WEBER MEDULLARY PLUG |
Generic Name | WEBER MEDULLARY PLUG |
Product Code | LZN |
Date Received | 2020-03-13 |
Model Number | N/A |
Catalog Number | UNKNOWN |
Lot Number | UNKNOWN |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ZIMMER GMBH |
Manufacturer Address | SULZER ALLEE 8 SULZER INDUSTRIE PARK WINTERTHUR 8404 SZ 8404 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization | 2020-03-13 |