FDA Adverse Event Injury Summary report: N

UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT

MDR report key: 24724647 · Received March 30, 2026

Report

Report Number
9610612-2026-00053
Event Type
Injury
Date Received
March 30, 2026
Report Date
May 25, 2026
Manufacturer
AESCULAP AG
Product Code
OOG
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

MANUFACTURING SITE EVALUATION: INVESTIGATION ON-GOING. ADDITIONAL INFORMATION / INVESTIGATION RESULTS WILL BE PROVIDED IN A SUPPLEMENTAL REPORT.

Description of Event or Problem · 0

AN ADVERSE EVENT WAS REPORTED INVOLVING AN UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT SYSTEM. SPECIFICALLY, IT WAS REPORTED THAT THERE WAS POSTOPERATIVE LOOSENING. A REVISION SURGERY HAD BEEN PLANNED. ACCORDING TO MANUFACTURER'S REPORTING EVALUATION IN ACCORDANCE WITH 21 CFR PART 803, SECTION 803.3, THIS EVENT IS CONSIDERED REPORTABLE FOR THE FOLLOWING REASON - ADVERSE EVENT (NOT LATER THAN 30 DAYS). THE ASSESSMENT FOR THE REPORTABILITY OF THIS ADVERSE EVENT WAS BASED ON THE PATIENT HARM, REVISION SURGERY. ADDITIONAL INFORMATION WAS NOT PROVIDED. THE ADVERSE EVENT IS FILED UNDER AESCULAP AG REFERENCE NO. (B)(4). ASSOCIATED MEDWATCH REPORTS: UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT (AESCULAP AG REFERENCE NO. (B)(4): 9610612-2026-00035), UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT (AESCULAP AG REFERENCE NO. (B)(4); 9610612-2026-00050), UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT (AESCULAP AG REFERENCE NO. (B)(4); 9610612-2026-00051), UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT (AESCULAP AG REFERENCE NO. (B)(4); 9610612-2026-00052), UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT (AESCULAP AG REFERENCE NO.(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
568746 UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT KNEE ENDOPROSTHETICS OOG AESCULAP AG UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention