FDA Recall Terminated

iTotal Hip Replacement System, Model number HAA-050-D020-020102 The Conformis Hip System includes standard hip replacement components as well as the following patient specific components: femoral stem and single use instrumentation.

Recall: Z-0475-2021 · Initiated September 21, 2020

Recall

Recall Number
Z-0475-2021
Event Number
86615
Firm
Conformis, Inc.
FEI Number
3009844603
Product Code
LPH
Status
Terminated
Root Cause
Process control
Initiated
September 21, 2020
Terminated
June 12, 2023
Address
600 Technology Park Dr, Billerica, MA, 01821-4154

Description

iTotal Hip Replacement System, Model number HAA-050-D020-020102 The Conformis Hip System includes standard hip replacement components as well as the following patient specific components: femoral stem and single use instrumentation.

Reason

Incorrect hip components were provided in kits.

Action

The firm received complaints regarding the mix-up of serial numbers on September 11, 2020, and September 21, 2020, from a sales representative who reported that the incorrect iView bearing serial number 0469255 was provided in the kit for serial number 0469225, and that the incorrect iJigs bearing serial number 0469225 were provided in the kit for serial number 0469255. One of the kits was used, while the other was returned to the firm. The firm reported that the co-mingle only involved these two kits. Upon notification of the issue, the firm implemented a planned deviation to verify that there were no other occurrences of the issue. All components were found to be associated with the correct serial number. If you have any questions, contact Director, Regulatory Affairs at 781-345-9001 or email: [email protected].

Distribution

US Distribution in CA.

Quantity

2