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Open, Classified

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

FDA Recall Z-1318-2024 · Posted 2024-03-20

Recalling FirmThink Surgical, Inc.
Recall StatusOpen, Classified
Product CodeOLO
Date Initiated2024-02-12
Product Quantity16

Reason for Recall

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.

Firm 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.

Root Cause

Device Design

Distribution Pattern

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

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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