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Lower risk Food recall · FDA · Published August 2, 2016

Good Neighbor Pharmacy Cranberry Tablets: Incorrect Calcium Label and Serving Size

Good Neighbor Pharmacy recalls Cranberry tablets due to incorrect calcium labeling and serving size on product labels. Consumers may be unaware of calcium content and receive incorrect dosage.

🇺🇸 FDA recall #F-2194-2016FoodGood Neighbor Pharmacy ›
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Recalling firmReese Pharmaceutical Company10617 Frank Ave · Cleveland, OH 44106-4218
✎ GovInfoNow plain-language explainer

What happened, in plain English

Good Neighbor Pharmacy is recalling Cranberry tablets that have incorrect calcium labeling and serving size. This could lead users to be unaware of calcium content and take an incorrect dose. Read more at govinfonow.com/recall/23677-good-neighbor-pharmacy-cranberry-tablets-incorrect-calcium-label-and-serving.

Source Summary by GovInfoNow · govinfonow.com/recall/23677-good-neighbor-pharmacy-cranberry-tablets-incorrect-calcium-label-and-serving · Updated October 9, 2026 · FDA enforcement record: FDA #F-2194-2016

Cite this page

“Good Neighbor Pharmacy Cranberry Tablets: Incorrect Calcium Label and Serving Size.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23677-good-neighbor-pharmacy-cranberry-tablets-incorrect-calcium-label-and-serving. Based on FDA recall #F-2194-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2194-2016%22&limit=1).

Why it’s dangerous

The product label does not include calcium, so users might not know they're getting calcium. The serving size is listed as 900mg but should be 500mg, which could lead to incorrect dosing.

Who’s affected

People who bought the Cranberry tablets from Good Neighbor Pharmacy. Those with calcium needs or urinary health concerns may be most at risk.

How to tell if you have this one

Check for the product name 'Cranberry Tablets, Cranberry Supplement 450mg. Urinary Health' on the carton. The lot number P15J478 with expiration date 10/1:17 is also listed.

  • Brand
    Good Neighbor Pharmacy
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Label

    Look for the product name and lot number on the carton to confirm if it's recalled.

Where it went and when

Where it was distributed

Distributed in 19 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: not listedWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: yesKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “AL, AZ, CA, FL, GA, HI, IL, KY, MA, MI, MN, MO, NC, OH, PA, TX, UT, VA, WA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arizona, California, Florida, Georgia, Hawaii, Illinois, Kentucky, Massachusetts, Michigan, Minnesota, Missouri, North Carolina, Ohio, Pennsylvania, Texas, Utah, Virginia, Washington.

Recall timeline

FDA terminated this recall 12 months after the firm started it.

1. Firm started the recall: Aug 2, 201612. FDA classified it Class III: Sep 14, 201623. Published in FDA’s Enforcement Report: Sep 21, 201634. FDA terminated the recall: Aug 2, 2017420162017
  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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Questions people ask

Is there a risk of serious injury from this product?

The recall indicates potential incorrect dosing, but no serious injury risk is mentioned.

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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 #F-2194-2016 (August 2, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2194-2016 to see it in context.
  • Plain-language summary written by qwen3:4b on October 9, 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