FDA Recall Open, Classified

Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System

Recall: Z-1318-2024 · Initiated February 12, 2024

Recall

Recall Number
Z-1318-2024
Event Number
94086
Firm
Think Surgical, Inc.
FEI Number
3000719653
Product Code
OLO
Status
Open, Classified
Root Cause
Device Design
Initiated
February 12, 2024
Posted
March 20, 2024
Address
47201 Lakeview Blvd, Fremont, CA, 94538-6530

Description

Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System

Reason

There is a galling effect (cold-weld) caused by friction between the array fixation pins and the TMINI array guide holes due to insufficient clearance between the outer diameter of the fixation pins and the inner diameter of the TMINI array guide holes. As a result, the array guide has the possibility of binding to the array fixation pins during drilling.

Action

On 2/12/24, recall notices were mailed and emailed to customers who were asked to do the following: 1) Examine your inventory, locate any unused devices and quarantine them immediately. Your clinical representative(s) will assist with the recall process and provide guidance to your surgeon(s) for positioning the array fixation pins using the array bracket. 2) Do not use any affected product and return any used or unused product. 3) Complete and return the acknowledgment form to [email protected] Customers with questions can contact the firm via phone at 510-249-2300, Option 1.

Distribution

US Nationwide distribution in the states of AL, OH, NV, TX, UT, CA, MO.

Quantity

16