MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-09-16 for UNKNOWN ZIMMER TM REVERSE GLENOSPHERE manufactured by Zimmer Inc.
[25991598]
Information was received via published literature. (b)(4). Other device used: catalog # unknown, unknown zimmer tm reverse polyethylene liner, lot # unknown. Catalog # unknown, unknown zimmer tm reverse base plate, lot # unknown. Please reference literature at the following location: http://www. Ncbi. Nlm. Nih. Gov/pmc/articles/pmc4168654/ operative notes were requested; however, none provided. Relevant medical history and adherence to rehabilitation protocol are unknown. No devices or photos were received; therefore, the condition of the components is unknown. The part and lot numbers of the product are unknown; therefore, the device history records could not be reviewed. The complaint history for these products could not be reviewed due to the lack of lot numbers. It could not be confirmed if the devices are an approved and compatible combination. A definitive root cause cannot be determined with the information provided. The investigation could not verify or identify any evidence of product contribution to the reported problem. Based on the available information, the need for corrective action is not indicated. Should additional information be received, the complaint will be reopened. Zimmer, inc. Considers the investigation closed.
Patient Sequence No: 1, Text Type: N, H10
[25991599]
It has been reported that 16 patients had scapular notching. Of these, 7 patients had grade 1 scapular notching, 7 patients had grade 2 notching, 1 had grade 3 and 1 had grade 4 notching.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1822565-2015-01887 |
| MDR Report Key | 5082468 |
| Date Received | 2015-09-16 |
| Date of Report | 2015-08-20 |
| Date Mfgr Received | 2015-08-20 |
| Date Added to Maude | 2015-09-16 |
| 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 | KEVIN ESCAPULE |
| Manufacturer Street | P.O. BOX 708 |
| Manufacturer City | WARSAW IN 465810708 |
| Manufacturer Country | US |
| Manufacturer Postal | 465810708 |
| Manufacturer Phone | 8006136131 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | UNKNOWN ZIMMER TM REVERSE GLENOSPHERE |
| Generic Name | SHOULDER PROSTHESIS |
| Product Code | KWR |
| Date Received | 2015-09-16 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ZIMMER INC |
| Manufacturer Address | P.O. BOX 708 WARSAW IN 465810708 US 465810708 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2015-09-16 |