Class IITerminated in FDA datasetAug 7, 2018

BLUE GREEN ALGAE: Packaged under the following brands: AMERICAN HEALTH KALMATH SHORES BLUE GREEN ALGAE, 120 CAPSULES

Recalling firm: Natures Bounty Inc

Why it was recalled

High level of microcystin observed in the product.

Check the codes ↓

The exact product

BLUE GREEN ALGAE: Packaged under the following brands: AMERICAN HEALTH KALMATH SHORES BLUE GREEN ALGAE, 120 CAPSULES, UPC: 0 76630 02542 3 and Puritan's Pride PREMIUM Kalamath Lake Blue Green Algae, 500 MG, 120 RAPID RELEASE CAPSULES, UPC 0 74312 12542 3

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Lot Number/Expiry Date: 178747 / 05/2020;199658 / 10/2020; 264855 / 04/2021; 33766 / 01/2020; 959219 / 02/2019; 964323 / 10/2018; 982016 / 04/2019; 982017 / 05/2019

TypeCode / valueContext
UPC074312125423PREMIUM Kalamath Lake Blue Green Algae, 500 MG, 120 RAPID RELEASE CAPSULES, UPC 0 74312 12542 3
UPC076630025423ing brands: AMERICAN HEALTH KALMATH SHORES BLUE GREEN ALGAE, 120 CAPSULES, UPC: 0 76630 02542 3 and Puritan's Pride PREMIUM Kalamath Lake Blue Green Algae, 500 MG, 120 RAPID RELEASE CAPSULES, UPC 0 74312 12542 3

Recall details

Recall number
F-1835-2018
Event ID
80781
FDA status
Terminated
Initiated
Aug 7, 2018
Reported
Aug 29, 2018
Classified
Aug 20, 2018
Terminated
Mar 20, 2019
Quantity
71,409 Bottles
Location
Ronkonkoma, NY, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide and Foreign: AUSTRALIA AUSTRIA BELGIUM CANADA CANADA CHILE CHINA COLOMBIA CROATIA DOMINICAN REPUBLIC ECUADOR ENGLAND FINLAND FRENCH POLYNESIA TAHITI GUATEMALA HONG KONG HUNGARY ICELAND ISRAEL ITALY JAMAICA JAPAN KAZAKHSTAN MACEDONIA MALAYSIA MEXICO MOLDOVA NETHERLANDS NEW ZEALAND PARAGUAY POLAND ROMANIA SCOTLAND SOUTH AFRICA SOUTH KOREA(ROK) SPAIN SWITZERLAND SWITZERLAND TAIWAN U.S.A. UGANDA VANUATU

FDA source record · F-1835-2018

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.