Roche recalls Accu-Chek Guide blood glucose monitors with model 08313202001 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 Accu-Chek Guide blood glucose monitors with model number 08313202001 that may have power issues. This could affect the device's reliability for diabetes monitoring, though the recall does not specify a fix or deadline.
The recall mentions potential power issues with the device, which could lead to inaccurate glucose readings. However, the specific mechanism of how power issues might occur or cause harm is not detailed in the notice.
People with diabetes who use the Accu-Chek Guide blood glucose monitoring system with model number 08313202001 are most at risk. The recall applies to units with serial numbers below XXX11000001.
Check for the model number 08313202001 on the device. Affected units have serial numbers starting with three digits followed by numbers below 11000001.
Look for the model number 08313202001 on the Accu-Chek Guide blood glucose monitor.
The recall notice does not specify any remedy for the power issues.
Check for the model number 08313202001 and serial numbers below XXX11000001.
The recall does not state that users should stop using the device.
We’ve drafted a message you can send Roche to request your refund or repair — edit it as you like.
Subject: Recall Z-0752-2020 — Roche Roche Hello, I own a Roche that is covered by recall Z-0752-2020 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.
