FDA recall record

Roche Diabetes Care Blood Glucose Monitoring System, Model Number 08453063001 ACCU-CHEK recall — FDA Z-0751-2020

Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.

Class IIclassification
Z-0751-2020official record ID
Jan 8, 2020report date

Recall record at a glance

Official recordZ-0751-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRoche Diabetes Care, Inc.
Report dateJan 8, 2020
Recall initiation dateSep 30, 2019
Quantity355,400
LocationIndianapolis, IN, United States

Official product description

Blood Glucose Monitoring System, Model Number 08453063001 ACCU-CHEK GUIDE SAMPLE KIT FCN MG/DL US - 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.

Why the product was recalled

Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.

Distribution information

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.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: N/A.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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