Medtronic Navigation, Inc. (Littleton)
Country not established
- Devices
- 1
- FDA recalls
- 202 ongoing
At a glance
Market reach
- United States
- FDA recalls
What Medtronic Navigation, Inc. (Littleton) makes
Medtronic Navigation, Inc. makes medical imaging systems, including the O-ARM IMAGING SYSTEM.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
O-Arm Imaging System Ref K092564
Regimes: 510(k) Registry: 510(k)
FDA recalls
FDA recall records list 20 recalls initiated by Medtronic Navigation, Inc. (Littleton), the earliest on 2016-03-17 and the most recent on 2024-04-26. By recorded status: 2 ongoing and 18 terminated. The reasons filed fall into these groups: labeling or instructions for use, software or firmware, electrical or power, performance or accuracy and manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 1
- 2018 12
- 2019 2
- 2020 0
- 2021 0
- 2022 0
- 2023 1
- 2024 1
- 2025 0
- 2026 0
2024
- 26 Apr 2024 Z-2026-2024 Class II Ongoing Potential for an electrical component of the O-arm" O2 Imaging System to intermittently shut off,failure can cause the potential for surgical delay, additional imaging, cancellation and rescheduling of surgery, or
completion of surgery without the benefit of image guidance.
Full distribution text
- 26 Apr 2024 Z-2026-2024 Class II Ongoing Potential for an electrical component of the O-arm" O2 Imaging System to intermittently shut off,failure can cause the potential for surgical delay, additional imaging, cancellation and rescheduling of surgery, or
completion of surgery without the benefit of image guidance.
2023
- 25 Jul 2023 Z-2449-2023 Class II Ongoing Ground cable installed incorrectly.
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- 25 Jul 2023 Z-2449-2023 Class II Ongoing Ground cable installed incorrectly.
2019
- 15 Nov 2019 Z-0767-2020 Class II Terminated Due to a manufacturing issue affecting particular O-arm" O2 Imaging Systems, Medtronic has determined that the gantry tractor motor drive belt may loosen over an extended number of uses at a higher frequency in these systems. If the belt loosens, it may result in rotation of 3D images about the gantry isocenter. While the 3D image is anatomically accurate within the image itself and may be used to confirm therapy, its electronic registered location may be rotated relative to the actual physical position of the patient.
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- 1 May 2019 Z-1932-2019 Class II Terminated The 0-arm 1000 Imaging System uses energy from the batteries to generate X-rays and move the system. If a charger board is not functioning properly, the batteries will not receive a full recharge of the potential capacity and results in the inability of the system to take X-rays, open the gantry, and move the system from one place to another, which may affect the ability to continue use within the operating room until the charger board and/or the batteries are replaced
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- 15 Nov 2019 Z-0767-2020 Class II Terminated Due to a manufacturing issue affecting particular O-arm" O2 Imaging Systems, Medtronic has determined that the gantry tractor motor drive belt may loosen over an extended number of uses at a higher frequency in these systems. If the belt loosens, it may result in rotation of 3D images about the gantry isocenter. While the 3D image is anatomically accurate within the image itself and may be used to confirm therapy, its electronic registered location may be rotated relative to the actual physical position of the patient.
2018
- 17 Sep 2018 Z-0404-2019 Class II Terminated O-arm 02 Imaging Systems correction to software version 4.1.0; new version of the user manual and an Image Acquisition System ("IAS") product label; replacing blown fuse of the new AC power input circuit
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- 30 Aug 2018 Z-0271-2019 Class II Terminated Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
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- 30 Aug 2018 Z-0272-2019 Class II Terminated Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
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- 30 Aug 2018 Z-0273-2019 Class II Terminated Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
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- 30 Aug 2018 Z-0274-2019 Class II Terminated Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
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- 30 Aug 2018 Z-0275-2019 Class II Terminated Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
Full distribution text
- 17 Sep 2018 Z-0404-2019 Class II Terminated O-arm 02 Imaging Systems correction to software version 4.1.0; new version of the user manual and an Image Acquisition System ("IAS") product label; replacing blown fuse of the new AC power input circuit
Show all 20 recalls
2018
- 30 Aug 2018 Z-0276-2019 Class II Terminated Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
Full distribution text
- 30 Aug 2018 Z-0277-2019 Class II Terminated Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
Full distribution text
- 30 Aug 2018 Z-0278-2019 Class II Terminated Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
Full distribution text
- 30 Aug 2018 Z-0279-2019 Class II Terminated Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
Full distribution text
- 30 Aug 2018 Z-0280-2019 Class II Terminated Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
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- 25 Jan 2018 Z-0928-2018 Class II Terminated Software update ("SW Update 3.2.1") is being implemented to address the following issues: Inability to power the system after shutdown, System stays in standalone mode, Image reconstruction, System/Pendant bootup, Dose display/report, Gantry motion, Network communication, System shutdown, and Early termination of 3D spin.
Full distribution text
- 30 Aug 2018 Z-0276-2019 Class II Terminated Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
2017
- 30 Sep 2017 Z-0927-2018 Class II Terminated During servicing of certain internal components of the O-Arm O2 Surgical Imaging System, it is possible that the high-power cable connector may come in contact with surrounding metal during the disconnecting/reconnecting process which may result in an electrical short and a shock to the field service technician.
Full distribution text
- 30 Sep 2017 Z-0927-2018 Class II Terminated During servicing of certain internal components of the O-Arm O2 Surgical Imaging System, it is possible that the high-power cable connector may come in contact with surrounding metal during the disconnecting/reconnecting process which may result in an electrical short and a shock to the field service technician.
2016
- 22 Sep 2016 Z-0070-2017 Class II Terminated O-arm O2 Surgical Imaging System Spatial calibration may be erroneous in Stealth Station navigated images
- 17 Mar 2016 Z-2082-2016 Class II Terminated It has been discovered that replacement x-ray generator and system motion batteries could become damaged during shipment, resulting in unacceptable risk of failure.
- 17 Mar 2016 Z-2083-2016 Class II Terminated Review of on-system electronic product labeling and Instr uctions for Use in response to an internal management concern uncovered gaps in compliance with the requirements for information to be provided to users in 21CFR part 1 020.30(h).
Frequently asked questions
How many devices does Medtronic Navigation, Inc. (Littleton) have in the registry?
The registry currently lists 1 device for Medtronic Navigation, Inc. (Littleton). Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Navigation, Inc. (Littleton)'s devices?
Among its 1 most recently registered device, Medtronic Navigation, Inc. (Littleton) has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic Navigation, Inc. (Littleton)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic Navigation, Inc. (Littleton)'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Medtronic Navigation, Inc. (Littleton)?
FDA recall records list 20 recalls initiated by Medtronic Navigation, Inc. (Littleton), the most recent initiated on 26 Apr 2024. 2 of them are recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Medtronic Navigation, Inc. (Littleton) in the registry?
The most recently registered devices listed for Medtronic Navigation, Inc. (Littleton) include O-ARM IMAGING SYSTEM.