VERSA-DIAL/COMP TI STD TAPER
Report
- Report Number
- 0001825034-2019-00926
- Event Type
- Injury
- Date Received
- March 1, 2019
- Date of Event
- September 11, 2018
- Report Date
- June 24, 2019
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- MBF
- PMA / PMN Number
- K060716
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4). THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL AND/OR CORRECTED INFORMATION. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DHR WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
(B)(4). CONCOMITANT MEDICAL PRODUCTS: PART # 113627, LOT # 292310, COMP PRIMARY STEM 7MM MINI; PART # 115310, LOT # 990660, COMP RVRS SHLDR GLNSP STD 36MM; PART # 110005273, LOT # 184150, COMP CNV GLEN BASE NON HA; PART # XL-115363, LOT # 588250 OR 145510, ARCOM XL 44-36 STD HMRL BRNG; PART # 115375, O5 115370, LOT # 822460, OR 272100 COMP RVS TRAY CO 44MM; PART # 115395, LOT # 650420 COMP RVS CNTRL 6.5X25MM ST/RST; PART # 180551, LOT # 969080, COMP LK SCR 3.5HEX 4.75X20 ST; PART # 180552, LOT # 715590, COMP LK SCR 3.5HEX 4.75X25 ST; PART # 405883, LOT # 538650, COMP RVS 3.2MM DRL; PART # 405800, LOT # 905620, COMP. REV SHLDR 9 IN STEINMANN; PART # 405889, LOT # 538820, COMP RVS 2.7MM DIA DRL; PART # 110005237, LOT # 509950, COMP CONV GLEN LINER E1. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 -2019 -00920, 0001825034 -2019 -00921, 0001825034 -2019 -00922, 0001825034 -2019 -00923, 0001825034 -2019 -00924, 0001825034 -2019 -00925. NOT RETURNED TO MANUFACTURER.
IT HAS BEEN REPORTED THAT PATIENT IS SUFFERING FROM CHRONIC PAIN AND NON FUNCTIONING JOINT (9) NINE MONTHS POST REVISION SURGERY. PATIENT IS UNDERGOING SEEKING CARE UNDER A PAIN MANAGEMENT SPECIALIST. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 174456 | VERSA-DIAL/COMP TI STD TAPER | PROSTHESIS, SHOULDER | MBF | ZIMMER BIOMET, INC. | N/A | 120880 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 56 YR | Required Intervention| S |