Blood Glucose Monitoring System, Model Number 07400926001 ACCU-CHEK GUIDE RETAIL 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
Check against the official notice below — it lists the full affected range.
Roche Diabetes Care, Inc. is recalling the Accu-Chek Guide Blood Glucose Monitoring System, Model Number 07400926001, due to potential power issues with the device. The recall affects approximately 215,259 units distributed nationwide in the United States and internationally across multiple countries including Canada, Australia, Japan, and many others. The affected devices are those with serial numbers below XXX11000001, where XXX represents the first three digits of the serial number.
The recall notice does not specify a remedy or recommended course of action for consumers who have this product.
Written by software from the official notice below. Not reviewed by a lawyer.
Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring System.
Reason for recall: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring System. Distribution: 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. Quantity: 215,259 Lot/code info: Model Number : 07400926001 Device Identifier: 00365702702042 All serial numbers below XXX11000001 (where XXX is the first 3 digits of the serial number).
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.