Severity
Moderate
Natures Bounty Inc issued this FDA Food recall on August 29, 2018. Classified as Moderate severity (Class II). Approximately 71,409 Bottles units are affected. The recall was issued because: High level of microcystin observed in the product.. This recall notice is sourced from official FDA Food enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
This FDA Food action (record #F-1835-2018) was formally reported on August 29, 2018, with the manufacturer initiating the action on August 7, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Natures Bounty Inc is listed as the recalling firm, operating out of Ronkonkoma, NY. Federal records indicate 71,409 Bottles units are affected.
The documented reason for this recall is: High level of microcystin observed in the product. Distribution data in the federal record shows the product reached: 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 …. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 8 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Severity
Moderate
Units Affected
71,409 Bottles
Related Recalls
6
0 from same agency
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
High level of microcystin observed in the product.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1835-2018 |
| Date reported | August 29, 2018 |
| Date initiated | August 7, 2018 |
| Recalling firm | Natures Bounty Inc |
| Units affected | 71,409 Bottles |
| Distribution | 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 JAMAI… |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
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Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.
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Compare this recall with Icosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle, … →
Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
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Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).