Dexcom recalls
Dexcom has 29 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 1 Jul 2026. 18 are still ongoing. 5 were reported in the last 12 months. The most frequent reason is device malfunction.
Total recalls 29 since 2016
Last 12 months 5 reported
Class I 16 55% of total
Ongoing 18 latest 1 Jul 2026
Recalls per month, last 24 months click a bar for that month
Severity split
Class I 16 55% Class II 13 45% Class III 0 0%
Ongoing dexcom recalls 18 active
All dexcom recalls, newest first 29 total
Reported Class Recall Company Reason Where 1 Jul 2026 Device CLASS II G7 Continuous Glucose Monitoring System Dexcom G7 US Retail recalled Dexcom Device Malfunction CA 20 May 2026 Device CLASS II ONE+ iOS CGM App recalled by Dexcom Dexcom Device Malfunction Nationwide 20 May 2026 Device CLASS II G7 Continuous Glucose Monitoring System Dexcom G7 CGM iOS App recalled Dexcom Device Malfunction Nationwide 20 May 2026 Device CLASS II G7 Continuous Glucose Monitoring System Dexcom G7 CGM watchOS App recalled Dexcom Device Malfunction Nationwide 5 Nov 2025 Device CLASS I G6 Continuous Glucose Monitoring System Dexcom G6 recalled Dexcom Device Malfunction Nationwide 10 Sep 2025 Device CLASS I G7 Continuous Glucose Monitoring System Dexcom G7 CGM iOS App recalled Dexcom Device Malfunction Nationwide 10 Sep 2025 Device CLASS I ONE+ iOS CGM App recalled by Dexcom Dexcom Device Malfunction Nationwide 10 Sep 2025 Device CLASS I G7 Continuous Glucose Monitoring System Dexcom G7 CGM watchOS App recalled Dexcom Device Malfunction Nationwide 10 Sep 2025 Device CLASS I ONE+ Android CGM App recalled by Dexcom Dexcom Device Malfunction Nationwide 10 Sep 2025 Device CLASS I G7 Continuous Glucose Monitoring System Dexcom G7 CGM Android App recalled Dexcom Device Malfunction Nationwide 25 Jun 2025 Device CLASS I G7 Glucose Receiver, SKUs recalled by Dexcom Dexcom Device Malfunction Nationwide 25 Jun 2025 Device CLASS I G6 Glucose Receiver, SKUs recalled by Dexcom Dexcom Device Malfunction Nationwide 25 Jun 2025 Device CLASS I One Continuous Glucose Monitoring System, SKUs recalled by Dexcom Dexcom Device Malfunction Nationwide 25 Jun 2025 Device CLASS I One+ Continuous Glucose Monitoring System recalled by Dexcom Dexcom Device Malfunction Nationwide 11 Jun 2025 Device CLASS II G7 iOS Application recalled by Dexcom Dexcom Other Nationwide 26 Feb 2025 Device CLASS II G6, Continuous Glucose Monitoring System recalled by Dexcom Dexcom Device Malfunction Nationwide 26 Feb 2025 Device CLASS II G6, Continuous Glucose Monitoring System, REFs: Stk-om recalled Dexcom Device Malfunction Nationwide 26 Feb 2025 Device CLASS II G6, Continuous Glucose Monitoring System recalled by Dexcom Dexcom Device Malfunction Nationwide 1 Apr 2020 Device CLASS II G5 Continuous Glucose Monitoring System The Dexcom G4 recalled Dexcom Foreign Material CA 1 Apr 2020 Device CLASS II G4 Platinum Continuous Glucose Monitoring System The Dexcom recalled Dexcom Foreign Material CA 1 Apr 2020 Device CLASS II G6 Continuous Glucose Monitoring System The Dexcom G4 recalled Dexcom Foreign Material CA 19 Feb 2020 Device CLASS II G6 CGM App for iOS recalled by Dexcom Dexcom Device Malfunction Nationwide 12 Feb 2020 Device CLASS II Dexcom Receiver, REF: MT22719, (Black, Pin, Blue), Rx Only recalled Dexcom Device Malfunction Nationwide 20 Apr 2016 Device CLASS I G4 Platinum Receiver with Share Receiver recalled by Dexcom Dexcom Device Malfunction Nationwide 20 Apr 2016 Device CLASS I G4 Platinum (Pediatric) Receiver with Share Receiver recalled by Dexcom Dexcom Device Malfunction Nationwide 20 Apr 2016 Device CLASS I G5 Mobile Receiver recalled by Dexcom Dexcom Device Malfunction Nationwide 20 Apr 2016 Device CLASS I G4 Platinum Receiver recalled by Dexcom Dexcom Device Malfunction Nationwide 20 Apr 2016 Device CLASS I G4 Platinum (Pediatric) Receiver recalled by Dexcom Dexcom Device Malfunction Nationwide 20 Apr 2016 Device CLASS I G4 Platinum (Professional) Receiver recalled by Dexcom Dexcom Device Malfunction Nationwide
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.