Medtronic Navigation, Inc.-Littleton recalls
Medtronic Navigation, Inc.-Littleton has 20 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 12 Jun 2024. 2 are still ongoing. The most frequent reason is device malfunction.
Total recalls 20 since 2016
Last 12 months 0 reported
Class I 0 0% of total
Ongoing 2 latest 12 Jun 2024
Recalls per month, last 24 months click a bar for that month Severity split
0 0%20 100%0 0%
Why medtronic navigation, inc.-littleton is recalled
Ongoing medtronic navigation, inc.-littleton recalls 2 active
All medtronic navigation, inc.-littleton recalls, newest first 20 total Reported Class Recall Company Reason Where 12 Jun 2024 Device CLASS II O-arm O2 Imaging System-Mobile x-ray system designed recalled Medtronic Navigation, Inc.-Littleton Device Malfunction Nationwide 30 Aug 2023 Device CLASS II The O-arm O2 Imaging System is a mobile x-ray system recalled Medtronic Navigation, Inc.-Littleton Other Nationwide 8 Jan 2020 Device CLASS II O-arm" O2 Imaging System, Product Number/CFN: BI recalled Medtronic Navigation, Inc.-Littleton Other 23 states 10 Jul 2019 Device CLASS II Medtronic 0-arm TM 1000 Imaging Systems recalled by Medtronic Navigation Medtronic Navigation, Inc.-Littleton Other Nationwide 14 Nov 2018 Device CLASS II Medtronic Navigation 0-arm 02 Imaging System interventional recalled Medtronic Navigation, Inc.-Littleton Device Malfunction Nationwide 31 Oct 2018 Device CLASS II O-arm 1000 2nd Edition Imaging System recalled by Medtronic Navigation Medtronic Navigation, Inc.-Littleton Device Malfunction 45 states 31 Oct 2018 Device CLASS II O-arm 1000 2nd Edition Imaging System recalled by Medtronic Navigation Medtronic Navigation, Inc.-Littleton Device Malfunction 45 states 31 Oct 2018 Device CLASS II O-arm 1000 2nd Edition Imaging System recalled by Medtronic Navigation Medtronic Navigation, Inc.-Littleton Device Malfunction 45 states 31 Oct 2018 Device CLASS II O-arm 1000 2nd Edition Imaging System recalled by Medtronic Navigation Medtronic Navigation, Inc.-Littleton Device Malfunction 45 states 31 Oct 2018 Device CLASS II O-arm 1000 2nd Edition Imaging System recalled by Medtronic Navigation Medtronic Navigation, Inc.-Littleton Device Malfunction 45 states
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About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.