Recall Register

Mako Surgical Corporation: FDA recalls

FDA enforcement reports name Mako Surgical Corporation as the recalling firm in 22 events. The events have 27 product records. The recalls started from 2012 to 2022. All the events are device recalls.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

22 events, newest first.

FDA enforcement events of Mako Surgical Corporation
InitiatedProduct (first record)TypeClassRecordsStatus
8 Aug 2022Stryker USB Converter, Polaris Spectra Camera, Catalog #201148, a component of the Mako Robotic-Arm Assisted Surgery System.DeviceClass II1Terminated
23 Oct 2020Mako Integrated Cutting System (MICS) Handpiece, Catalog Number 209063, Software Version#: THA 3.0 and later, PKA 3.0 and later, and TKA 1.0 - Product Usage: The MICS Handpiece is attached to the distal end of the robotic arm and is used to register the RIO (Mako robot) and to execute bone preparation during a Mako…DeviceClass II1Completed
9 Jul 2020Mako Hip End Effector, Variable Angle Catalog Number: 206967 GTIN:00848486022167DeviceClass II1Terminated
25 Apr 20192.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only)DeviceClass II2Terminated
24 Jul 2018Stryker Mako Vizadisc Knee Procedure Tracking KitDeviceClass II2Terminated
10 May 2018Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Application (PKA) for use with the Robotic Arm Interactive Orthopedic System (RIO) is intended to assist the surgeon in providing software defined spatial boundaries for orientation and reference information to anatomical…DeviceClass II1Terminated
19 Jan 2018Restoris MCK Onlay Insert Extractor.DeviceClass II1Terminated
27 Dec 2017Makoplasty RIO Standard System; Ethernet to Fiber Optic Converter Catalog # 200933 Product Usage: The Partial Knee Application (PKA), for use with the Mako System, is indicated for use in surgical knee procedures, in which the use of stereotactic surgery may be appropriate, and where reference to rigid anatomical…DeviceClass II1Terminated
1 Dec 2017RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.DeviceClass II1Terminated
7 Aug 2017Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is intended to assist the surgeon in providing software define spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures.DeviceClass II2Terminated
7 Jun 2017MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software defined spatial boundaries during orthopedic procedures.DeviceClass II1Terminated
22 Dec 2016MAKO RIO THA Application User Guides, for total hip arthroplasty, orthopedic surgery.DeviceClass II1Terminated
29 Sep 2016Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components during acetabular reaming in MAKO Total Hip procedures.DeviceClass II1Terminated
23 Feb 2016RESTORIS PST RIO Offset Shell Impactor For use by orthopedic surgeons specifically for the purpose of positioning and implanting acetabular cup components during Total Hip Arthroplasty (THA) surgery.DeviceClass II1Terminated
15 Jan 2016Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for single or multi-compartmental knee replacement used in conjunction with RIO.DeviceClass II1Terminated
25 Nov 2015MAKOplasty Hip Array Kit Laminate 150230DeviceClass II1Terminated
16 Jul 2015Robotic Arm Interactive Orthopedic (RIO) system component PN#205143 (locking pin) and PN# 112220 (connector). Indicated for use in surgical knee resurfacing and total hip Arthroplasty joint replacement procedures.DeviceClass II1Terminated
22 Jan 2015Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System (RIO), is indicated for use in surgical knee procedures.DeviceClass II1Terminated
7 Oct 2014RESTORIS PST Straight Shell Inserter An impactor is a reusable instrument designed for use by orthopedic surgeons specifically for the purpose of positioning and implanting acetabular cup components during Total Hip Arthroplasty (THA) surgery.DeviceClass II3Terminated
30 Apr 2014Robotic Arm Interactive Orthopedic System (RIO)DeviceClass II1Terminated
9 Jan 2014Restoris Multicompartmental Knee (MCK) System is an implant system designed to be used with MAKO's Robotic Arm Interactive Orthopedic System (RIO). It is composed of a unicompartmental implant system (Restoris MCK Uni) and a patellofemoral implant system (Restoris MCK PF). The Restoris MCK Uni is designed for use…DeviceClass II1Terminated
12 Sep 2012The RIO (TGS 2.), Model # MAKO TGS 2.0 (Part No. 204000). The RIO is intended to assist the surgeon in providing software defined spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures. The RIO is indicated for use in surgical knee and hip procedures, in…DeviceClass II1Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

Mako Surgical Corporation: events for each product type
TypeEvents
Device22
Mako Surgical Corporation: events in each class
ClassEvents
Class II22
Share of the events of the firm in Class I
0%
Share of all events on the register in Class I
18%
Events with the status Ongoing
0

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Mako Surgical Corporation, by the year that the recall started. The largest year is 2016, with 4 events.

Official channels

Cite this page

Recall Register. Mako Surgical Corporation: FDA recalls. https://recallregister.com/firm/mako-surgical-corporation/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
FL

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Mako Surgical Corporation have?
Class II: 22 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Mako Surgical Corporation?
FDA event 90727, which the firm started on 8 Aug 2022. The first product in the record is: Stryker USB Converter, Polaris Spectra Camera, Catalog #201148, a component of the Mako Robotic-Arm Assisted Surgery System.
How many FDA recalls of Mako Surgical Corporation have the status Ongoing?
No event has the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.