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Roche Diabetes Care, Inc. recalls Blood Glucose Monitoring System, Model Number 07400870001 ACCU-CHEK GUIDE SAMPLE KIT MG/DL - Product Usage: The Accu-Ch
Recalled January 8, 2020 · FDA recall Z-0747-2020 · Roche Diabetes Care
Hazard
Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring System. · FDA Class II
Units
318,678
Sold at
US Nationwide distribution and countries of AR, AT, AU, BE, BR, CA, CH, CL, DE, DK, EC, ES, FI, FR, GB, GR, HK, HR, ID, IN, IT, JP, KR, LB, LT, LU, MM, MY, NL, NO, PH, PK, PT, SE, SG, TH, TW, ZA.
Description
Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring System.
Product
Blood Glucose Monitoring System, Model Number 07400870001 ACCU-CHEK GUIDE SAMPLE KIT MG/DL - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm as an aid in monitoring the effectiveness of glucose control. The Accu-Chek Guide blood Glucose Monitoring System is intended for in vitro diagnostic single-patient use by people with diabetes. The Accu-Chek Guide Blood Glucose Monitoring System is intended to be used by a single person and should not be shared.
Manufacturer(s)
Roche Diabetes Care, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →