M2A-MAGNUM TAPER INSERT
Report
- Report Number
- 0001825034-2020-00026
- Event Type
- Injury
- Date Received
- January 3, 2020
- Date of Event
- December 9, 2019
- Report Date
- April 10, 2020
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- KWA
- PMA / PMN Number
- K042037
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SC, US
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4). UPON RECEIPT OF ADDITIONAL INFORMATION IT HAS BEEN DETERMINED THAT THIS DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE REPORTED EVENT.
UPON RECEIPT OF ADDITIONAL INFORMATION IT HAS BEEN DETERMINED THAT THIS DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE REPORTED EVENT.
(B)(4). CONCOMITANT MEDICAL PRODUCTS: TAPERLOC POR LAT FMRL 11X142 CAT# 11-103205 LOT# 188920, M2A-MAGNUM PF CUP 54ODX48ID CAT# US157854 LOT# 921250, M2A-MAGNUM MOD HD SZ 48MM CAT# 157448 LOT# 721120. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS; HOWEVER, AN INVESTIGATION OF THE REPORTED EVENT IS IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETED, A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 -2020 -00023, 0001825034 -2020 -00024, 0001825034 -2020 -00025.
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL RIGHT HIP ARTHROPLASTY. SUBSEQUENTLY THE PATIENT WAS REVISED APPROXIMATELY 10 YEARS LATER DUE TO PAIN AND ELEVATED METAL ION LEVELS. THE FEMORAL HEAD AND TAPER ADAPTER WERE REMOVED AND REPLACED. 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 |
|---|---|---|---|---|---|---|---|
| 5487 | M2A-MAGNUM TAPER INSERT | PROSTHESIS, HIP | KWA | ZIMMER BIOMET, INC. | NI | 060800 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R |