UNK TM BASEPLATE
Report
- Report Number
- 0001822565-2020-01238
- Event Type
- Injury
- Date Received
- April 8, 2020
- Report Date
- April 1, 2020
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- HSD
- PMA / PMN Number
- NI
- Removal / Correction Number
- NI
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4). REPORT SOURCE: MIA S. HAGEN, MD, SACHIN ALLAHABADI, MD, ALAN L. ZHANG, MD, BRIAN T. FEELEY, MD, TREVOR GRACE, MD, C. BENJAMIN MA, MD* (2019). A RANDOMIZED SINGLE-BLINDED TRIAL OF EARLY REHABILITATION VERSUS IMMOBILIZATION AFTER REVERSE TOTAL SHOULDER ARTHROPLASTY, JOURNAL OF SHOULDER AND ELBOW ARTHROPLASTY. VOLUME 29, ISSUE 3, P442-450, HTTPS://DOI.ORG/10.1016/J.JSE.2019.10.005. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001822565 - 2020 - 01239. NO PRODUCT WAS RETURNED; VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. UNABLE TO PERFORM A COMPATIBILITY CHECK. MEDICAL RECORDS WERE NOT PROVIDED. PART AND LOT IDENTIFICATION ARE NECESSARY FOR REVIEW OF DEVICE HISTORY RECORDS, NEITHER WERE PROVIDED. A DEFINITIVE ROOT CAUSE COULD NOT BE DETERMINED. IF ANY FURTHER INFORMATION WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL REPORT WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.
THE STUDY REPORTED ONE PATIENT WITHIN THE IMMEDIATE-THERAPY GROUP HAD A GLENOSPHERE DISSOCIATION REQUIRING REVISION SURGERY AT 1-MONTH POSTOPERATIVELY. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 402547 | UNK TM BASEPLATE | PROSTHESIS, EXTREMITIES | HSD | ZIMMER BIOMET, INC. | NI | UNKNOWN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R |