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Lower risk Drug recall · FDA · Published February 2, 2017

Sage Products Q Care Continue Care Kit: Incorrect Expiration Date Risk

Sage Products recalls Q Care Continue Care Kit for non-ventilated patients due to incorrect expiration date printed on the kit. The kit expires November 13, 2017 instead of August 28, 2017. Consumers should check their kit's expiration date and contact Sage for details.

🇺🇸 FDA recall #D-0489-2017DrugSage Products ›
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Recalling firmSage Products Inc3909 3 Oaks Rd · Cary, IL 60013-1804
✎ GovInfoNow plain-language explainer

What happened, in plain English

Sage Products is recalling Q Care Continue Care Kits for non-ventilated patients because the expiration date printed on the kit is incorrect. The kit shows an expiration date of November 13, 2017, but the correct expiration date is August 28, 2017. Using this kit past its correct expiration date could lead to ineffective treatment. Read more at govinfonow.com/recall/42060-sage-products-q-care-continue-care-kit-incorrect-expiration-date.

Source Summary by GovInfoNow · govinfonow.com/recall/42060-sage-products-q-care-continue-care-kit-incorrect-expiration-date · Updated October 8, 2026 · FDA enforcement record: FDA #D-0489-2017

Cite this page

“Sage Products Q Care Continue Care Kit: Incorrect Expiration Date Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/42060-sage-products-q-care-continue-care-kit-incorrect-expiration-date. Based on FDA recall #D-0489-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0489-2017%22&limit=1).

Why it’s dangerous

The kit's expiration date is printed incorrectly as November 13, 2017, instead of the correct August 28, 2017. This means the kit may become ineffective after the correct expiration date, potentially leading to inadequate treatment for the patient.

Who’s affected

Patients using Q Care Continue Care Kits for non-ventilated patients who purchased the kit with the incorrect expiration date. Those most at risk are individuals who rely on the kit for medical treatment and may not notice the expiration date error.

How to tell if you have this one

Check the expiration date on the Q Care Continue Care Kit label. The kit should show an expiration date of November 13, 2017, but the correct date is August 28, 2017. The kit contains 1 Covered Yankauer and 2 Suction Toothbrush packages.

  • Brand
    Sage Products
  • Product
    Q Care Continue Care Kit for the non-ventilated patient; kit contains 1 Covered Yankauer, 2 Suction Toothbrush packages
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Expiration Date

    Look for the expiration date printed on the kit label. The kit shows November 13, 2017, but the correct expiration date is August 28, 2017.

Where it went and when

Where it was distributed

Distributed nationwide.

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: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 19 months after the firm started it.

1. Firm started the recall: Feb 2, 201712. FDA classified it Class III: Feb 21, 201723. Published in FDA’s Enforcement Report: Mar 1, 201734. FDA terminated the recall: Aug 28, 2018420172018
  1. Firm started the recall
  2. FDA classified it Class III
  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.

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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 #D-0489-2017 (February 2, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0489-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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