Dexcom Inc - Dexcom G4 PLATINUM Continuous Glucose Monitoring System - Class 2 Recall
Dexcom G4 PLATINUM Continuous Glucose Monitoring System The Dexcom G4 PLATINUM Continuous Glucose Monitoring System is a glucose monitoring device indicated for detecting trends and tracking patterns in persons (age 18 and older) with diabetes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 26, 2020 Category: Medical Devices Source Type: alerts

Dexcom Inc - Dexcom G6 Continuous Glucose Monitoring System - Class 2 Recall
Dexcom G6 Continuous Glucose Monitoring System The Dexcom G4 PLATINUM Continuous Glucose Monitoring System is a glucose monitoring device indicated for detecting trends and tracking patterns in persons (age 18 and older) with diabetes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 26, 2020 Category: Medical Devices Source Type: alerts

Dexcom Inc - Dexcom G5 Continuous Glucose Monitoring System - Class 2 Recall
Dexcom G5 Continuous Glucose Monitoring System The Dexcom G4 PLATINUM Continuous Glucose Monitoring System is a glucose monitoring device indicated for detecting trends and tracking patterns in persons (age 18 and older) with diabetes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 26, 2020 Category: Medical Devices Source Type: alerts

Insulet Corporation - Omnipod DASH Personal Diabetes Manager (PDM) - Class 2 Recall
Omnipod DASH Personal Diabetes Manager (PDM), Catalog numbers US: 18239 M/D: PDM-USA1-D001-MG-USA1 EU: PT-000010 - M/D: INT1-D001-MG PT-000011 M/D: INT1-D001-MM UDI 10385082000009 The Omnipod DASH Personal Diabetes Manager (PDM) is a mobile, handheld Android device that is intended to communicate with the Omnipod DASH Pod (pump). (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 21, 2020 Category: Medical Devices Source Type: alerts

Gentell, Inc - Gentell Hydrogel Ag - Class 2 Recall
Gentell Hydrogel Ag 4oz. Tube, model no. - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Silver Antimicrobial Wound Dressing is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 6, 2020 Category: Medical Devices Source Type: alerts

Gentell, Inc - Gentell Hydrogel Ag - Class 2 Recall
Gentell Hydrogel Ag 4x4, model no. GEN-11420 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 6, 2020 Category: Medical Devices Source Type: alerts

Gentell, Inc - Gentell Hydrogel Ag - Class 2 Recall
Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 6, 2020 Category: Medical Devices Source Type: alerts

Gentell, Inc - Gentell Hydrogel Ag - Class 2 Recall
Gentell Hydrogel Ag 2x2, model no GEN-11220 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second degree burns and skin tears. It provides a moist wound environment for healing. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 6, 2020 Category: Medical Devices Source Type: alerts

Abbott Diabetes Care, Inc. - Optium EZ Blood Glucose Monitoring System - Class 2 Recall
Optium EZ Blood Glucose Monitoring System, UDI: 00093815710653 (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 29, 2020 Category: Medical Devices Source Type: alerts

Abbott Diabetes Care, Inc. - Precision Xtra Blood Glucose & Ketone Monitoring System - Class 2 Recall
Precision Xtra Blood Glucose & Ketone Monitoring System, UDI: 00093815715023, 00093815988144 (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 29, 2020 Category: Medical Devices Source Type: alerts

Abbott Diabetes Care, Inc. - FreeStyle Precision H Blood Glucose and Ketone Monitoring System - Class 2 Recall
FreeStyle Precision H Blood Glucose and Ketone Monitoring System, UDI: 00093815711810 (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 29, 2020 Category: Medical Devices Source Type: alerts

Roche Diabetes Care, Inc. - The AccuChek Aviva Plus Test Strips - Class 2 Recall
Accu-Chek Aviva Plus Retail Strips 50 ct - intended for Blood Glucose Monitoring System Catalog Number: 06908217001 (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 6, 2020 Category: Medical Devices Source Type: alerts

Roche Diabetes Care, Inc. - AccuChek Aviva Plus Test Strips are for use with the AccuChek Aviva Blood Glucose Meter - Class 2 Recall
Accu-Chek Aviva Plus Health Network Strips- intended for Blood Glucose Monitoring System Catalog Number: 06908349001 (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 6, 2020 Category: Medical Devices Source Type: alerts

Roche Diabetes Care, Inc. - ACCUCHEK AVIVA ASPAC STRIP - Class 2 Recall
ACCU-CHEK AVIVA ASPAC STRIP 50CT- intended for Blood Glucose Monitoring System Catalog Number: 06453970020 (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 6, 2020 Category: Medical Devices Source Type: alerts

Dexcom Inc - Dexcom G5 Mobile Receiver - Class 2 Recall
Dexcom Receiver, REF: MT22719, (Black, Pin, Blue), Rx Only, containing software version SW10617 and revision 4.0.1.048 - Product Usage: A non-adjunctive invasive glucose sensor is intended to determine glucose levels, and the direction and rate of change of glucose levels in people with diabetes. The device is indicated to replace information obtained from standard blood glucose monitoring devices to make diabetes-related treatment decisions. The device also provides historical glucose information, facilitating long-term therapy adjustments. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 1, 2020 Category: Medical Devices Source Type: alerts