M2A-MAGNUM 42-50 TAPER INSRT STD
Report
- Report Number
- 0001825034-2020-01197
- Event Type
- Injury
- Date Received
- March 20, 2020
- Date of Event
- February 21, 2020
- Report Date
- July 8, 2020
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- KWA
- PMA / PMN Number
- K042037
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WI, US
- Reporter Occupation
- PHYSICIAN
Narratives
UPON FURTHER ASSESSMENT IT WAS DETERMINED THAT THE INFECTION OCCURRED GREATER THAN ONE YEAR POST-OPERATIVELY. THEREFORE, THIS EVENT IS NOT REPORTABLE AND SHOULD BE VOIDED.
UPON FURTHER ASSESSMENT IT WAS DETERMINED THAT THE INFECTION OCCURRED GREATER THAN ONE YEAR POST-OPERATIVELY. THEREFORE, THIS EVENT IS NOT REPORTABLE AND SHOULD BE VOIDED.
(B)(4). CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION AS THE PRODUCT WAS NOT RETURNED BY PATIENT. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. CONCOMITANT MEDICAL PRODUCTS: ITEM # 157446/ HEAD/ /LOT # 368210 . ITEM # 192012/ STEM / /LOT # 011470. ITEM # US157852/CUP/ LOT # 213330. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 -2020- 01198. 0001825034 -2020 -01199. 0001825034 -2020 -01200.
IT WAS REPORTED PATIENT UNDERWENT HIP REVISION SURGERY DUE TO INFECTION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 321840 | M2A-MAGNUM 42-50 TAPER INSRT STD | PROSTHESIS, HIP | KWA | ZIMMER BIOMET, INC. | NI | 004320 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R | SEE H10 |