Check the Batch
Class IITerminated in FDA datasetRecall initiated Aug 7, 2018

BLUE GREEN ALGAE: Packaged under the following brands: AMERICAN HEALTH KALMATH SHORES BLUE…

Recalling firm: Natures Bounty Inc

Why it was recalled

High level of microcystin observed in the product.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 20, 2019.

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Compare the exact product and package details with the label you have.

ProductBLUE 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
UPC074312125423, 076630025423

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

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

Extracted codes and context

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

Original FDA recall reason

High level of microcystin observed in the product.

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 ↗

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