Recall Z-0356-2014— Restoration Robotics

Name: FDA recall Z-0356-2014
Creator: U.S. Food and Drug Administration
Published: 2013-10-13

Class II · Terminated

Class II FDA medical device recall by Restoration Robotics, initiated 2013-10-13, terminated 2013-12-10. It names one FDA 510(k) clearance: K123548. Product: ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384; Inner Needle with Vacuum Tube FP-45385; dissection Punch 4.0mm FP 23304; Saline Nose Cone FP-45387; Follicle Trap FP 23306; Non-Sterile Disposable kit FP 23267 and Molded Parts, Reusable Kit FP 45538 Rx): Product Usage: Skin Tensioner is applied to patients scalp during follicular harvesting during hair restoration procedure. Product applies tension to scalp to facilitate follicular extractions.. Reason: Reports of discoloration (residue) on the pins of the skin tensioner have been received by several customers. Discoloration due to insufficient cleaning of stainless steel pins during passivation process. The residue has been identified as a compound of iron and chlorine..

Recalling firm: Restoration Robotics
Classification: Class II
Status: Terminated
Initiated: 2013-10-13
Terminated: 2013-12-10
Firm location: San Jose, CA, United States

510(k) clearances named in this recall

1 on FDA's record

K123548 — THE ARTAS SYSTEMRestoration Robotics, Inc.·cleared 2013-02-25

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384; Inner Needle with Vacuum Tube FP-45385; dissection Punch 4.0mm FP 23304; Saline Nose Cone FP-45387; Follicle Trap FP 23306; Non-Sterile Disposable kit FP 23267 and Molded Parts, Reusable Kit FP 45538 Rx): Product Usage: Skin Tensioner is applied to patients scalp during follicular harvesting during hair restoration procedure. Product applies tension to scalp to facilitate follicular extractions.

Reason for recall

Reports of discoloration (residue) on the pins of the skin tensioner have been received by several customers. Discoloration due to insufficient cleaning of stainless steel pins during passivation process. The residue has been identified as a compound of iron and chlorine.

Data sourced from openFDA. This site is unofficial and independent of the FDA.