Roche recalls Accu-Chek Guide Blood Glucose Monitoring System (model 07400870001) due to potential power issues. Affected units have serial numbers below XXX11000001. No remedy specified in recall notice.
Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring System.
Roche is recalling its Accu-Chek Guide Blood Glucose Monitoring System (model 07400870001) because of potential power issues. This could affect people with diabetes who rely on the device for blood glucose monitoring.
The recall states potential power issues with the device, but does not specify what these issues could cause. Without details on the hazard mechanism, it's unclear how this affects safety.
People with diabetes who use the Accu-Chek Guide Blood Glucose Monitoring System are most at risk. The device is intended for single-patient use only and should not be shared.
Check for the model number 07400870001 on the device. Affected units have serial numbers below XXX11000001 (where XXX are the first three digits of the serial number).
Look for the serial number on the device; affected units have numbers below XXX11000001 (where XXX is the first three digits).
The recall states potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System, but does not specify the exact hazard or what it could cause.
Model number 07400870001 with serial numbers below XXX11000001 (where XXX is the first three digits of the serial number).
The recall does not specify a remedy, so there is no instruction to stop using the device. However, the potential power issues may warrant checking the serial number.
We’ve drafted a message you can send Roche to request your refund or repair — edit it as you like.
Subject: Recall Z-0747-2020 — Roche Roche Hello, I own a Roche that is covered by recall Z-0747-2020 from Roche. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
