CLASS III Food recall · Reported 21 Sep 2016 · FDA Enforcement Report

Good Neighbor Pharmacy Cranberry Tablets, Cranberry Supplement 450mg recalled

Reese Pharmaceutical is recalling Good Neighbor Pharmacy Cranberry Tablets, Cranberry Supplement 450mg, distributed in 19 states. The recall was initiated on 2 Aug 2016 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot P15J478, Expiration 10/17

Quantity recalled2,880 finished goods

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-2194-2016
FDA event ID: 74854
Recalling firm: Reese Pharmaceutical, Cleveland, OH
Brand: Good Neighbor
Classification: Class III
Status: Terminated
Recall initiated: 2 Aug 2016
FDA classified: 14 Sep 2016
Reported: 21 Sep 2016
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Other Reasons
Product category: Dietary Supplements

Timeline

2 Aug 2016	Recall initiated by company
14 Sep 2016	Classified by FDA	+43 days
21 Sep 2016	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The finished product label on the Cranberry supplement does not include Calcium. Users of the product may be unaware of the Calcium in the supplement. Additionally the amount per serving as written on the product label is incorrect and should be 500mg, not 900mg.

Product as listed by the FDA

Good Neighbor Pharmacy Cranberry Tablets, Cranberry Supplement 450mg. Urinary Health. Tablets are packed in a labeled carton, 50 tablets per carton. Distributed by Amerisource Bergen 1300 Morris Drive Chesterbrook, PA 19087.

Where it was distributed

AL, AZ, CA, FL, GA, HI, IL, KY, MA, MI, MN, MO, NC, OH, PA, TX, UT, VA, WA

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

Questions about this recall

Why was it recalled?

Which lots are affected?

Lot P15J478, Expiration 10/17

Where was it sold?

AL, AZ, CA, FL, GA, HI, IL, KY, MA, MI, MN, MO, NC, OH, PA, TX, UT, VA, WA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Reese Pharmaceutical

All 3

Reported	Class	Recall	Company	Reason	Where
6 Dec 2017Food	CLASS II	Orange Flavor Immune Support Dietary Supplement Effervescent Tablets recalled	Reese Pharmaceutical	Other	40 states
6 Dec 2017Food	CLASS II	Berry Flavor Immune Support Dietary Supplement Effervescent Tablets recalledBerry Flavor	Reese Pharmaceutical	Other	40 states

Other Dietary Supplements recalls

All 733

Reported	Class	Recall	Company	Reason	Where
21 Sep 2026Food	ANNOUNCED	Niwali Tejocote Capsules and Pieces recalled by Global MixNiwali	Global Mix	Foreign Material	Nationwide
2 Sep 2026Food	CLASS I	Addall XR Shot, liquid dietary supplement recalled by ZMB EnterprisesAddall XR	ZMB Enterprises	Hidden Drug Ingredients	CA
5 Aug 2026Food	CLASS II	Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island	Mellish Island	Other	Nationwide
29 Jul 2026Food	CLASS I	Modern Warrior Ready, Dietary Supplement recalledModern Warrior	Modern Warrior Life	Hidden Drug Ingredients	Nationwide
8 Jul 2026Food	CLASS II	Vista MAX; Dietary Supplement Serving Size recalled by Provision HealthVista MAX	Provision Health	Undeclared Allergens	CA