UNK CONTINUUM CUP
Received Jun 29, 2026
Report 0001822565-2026-02305 · MDR key 25650515
Device
Generic name
Prosthesis, Hip
Manufacturer
Zimmer Biomet, Inc.Catalog number
UNK CONTINUUM CUP
Lot number
UNK
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Bone Fracture(s)
Narrative
Description of Event or Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE ON AN UNKNOWN DATE WHERE CPT AND CONTINUUM WAS IMPLANTED. SUBSEQUENTLY, THE PATIENT FELL AND EXPERIENCED A BONE FRACTURE. ADDITIONAL SURGERY WAS REQUIRED ON AN UNKNOWN DATE. A DE PUY PLATE WAS USED FOR FRACTURE. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Additional Manufacturer Narrative
(B)(4). G2: FOREIGN: NEW ZEALAND. THE CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION AS ITS LOCATION IS UNKNOWN. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED.