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Lower risk Medical device recall · FDA · Published June 8, 2017

Roche Accu-Chek Connect App: Rare Bolus Advisor Timer Error

Roche recalls Accu-Chek Connect diabetes app versions with rare timer error affecting insulin dosing advice. Users may need to restart app after pairing meter for first time.

🇺🇸 FDA recall #Z-0197-2018Medical deviceRoche ›
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Recalling firmRoche Diabetes Care, Inc.9115 Hague Rd · Indianapolis, IN 46256-1025
✎ GovInfoNow plain-language explainer

What happened, in plain English

Roche is recalling specific versions of its Accu-Chek Connect diabetes management app due to a rare bug in the Bolus Advisor feature. This error may cause the countdown timer to not display after initial meter pairing, potentially delaying insulin correction advice for recent blood glucose readings. Read more at govinfonow.com/recall/73897-roche-accu-chek-connect-app-rare-bolus-advisor-timer-error.

Source Summary by GovInfoNow · govinfonow.com/recall/73897-roche-accu-chek-connect-app-rare-bolus-advisor-timer-error · Updated September 23, 2026 · FDA enforcement record: FDA #Z-0197-2018

Cite this page

“Roche Accu-Chek Connect App: Rare Bolus Advisor Timer Error.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/73897-roche-accu-chek-connect-app-rare-bolus-advisor-timer-error. Based on FDA recall #Z-0197-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0197-2018%22&limit=1).

Why it’s dangerous

The app error can cause the countdown timer to disappear after initial meter pairing, making correction bolus advice unavailable for the most recent valid glucose reading. This may delay insulin dosing advice, but the error is rare and only occurs after the first pairing.

Who’s affected

Diabetes patients using the affected Accu-Chek Connect app versions on iOS or Android. Those who have paired their glucose meter with the app for the first time may experience the rare timer error.

How to tell if you have this one

Check if you have the Accu-Chek Connect app version 1.0.5, 1.0.15, 1.2.0, 1.2.2, 1.2.3, 2.0.0, 2.0.1, 2.1.0, or 2.1.1 for iOS or Android. The app was sold with specific catalog numbers: 07562462001 / GTIN 00365702700000 or 07250452001 / GTIN 00365702700017.

  • Brand
    Roche
  • Product
    Accu-Chek Connect diabetes management software app, Catalog number 07562462001 / GTIN number 00365702700000, Catalog
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check App Version

    Verify your Accu-Chek Connect app version by checking the app store settings or the app's version number.

  2. Restart App After Pairing

    If you paired your glucose meter with the app for the first time, restart the app to see if the countdown timer displays correctly.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Worldwide Distribution - US (Nationwide) and Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 14 months after the firm started it.

1. Firm started the recall: Jun 8, 201712. FDA classified it Class II: Dec 6, 201723. Published in FDA’s Enforcement Report: Dec 13, 201734. FDA terminated the recall: Aug 6, 2018420172018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Do I need to update the app?

The recall does not require updating the app. Restarting after initial pairing may resolve the issue.

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Where this comes from

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.

  • Official source: FDA Recall #Z-0197-2018 (June 8, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0197-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA