ALLEN PLUG
Received Jul 21, 2026
Report 0001822565-2026-02643 · MDR key 25888960
Device
Generic name
Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented
Manufacturer
Zimmer Biomet, Inc.Catalog number
00801102032
Lot number
66528224
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Female
- Insufficient Information
Narrative
Additional Manufacturer Narrative
(B)(4). D10: CAT#: 00585004603, LOT#: 67753852, CAT#: 00585003014, LOT#: 66601091, CAT#: 00585204030, LOT#: 67348514, CAT#: 00598801016, LOT#: 67638151, CAT#: 00585205014, LOT#: 67740616, CAT#: 00585004604, LOT#: 66018620, CAT#: 00585001396, LOT#: 67536093, CAT#: 00588000500, LOT#: 67243960, CAT#: 00585004301, LOT#: 67524738, CAT#: 00223200418, LOT#: 67849377. G2: FOREIGN - EVENT OCCURRED IN AUSTRALIA. 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.
Description of Event or Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT A KNEE SURGERY AND SUBSEQUENTLY PASSED AWAY IN THE FOLLOWING DAYS OF THE PROCEDURE, ON AN UNKNOWN DATE, DUE TO UNKNOWN MEDICAL COMPLICATIONS. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.