PlainRecalls
ModerateClass IITerminated

FDA Food recall · Reported April 6, 2016

All Day Energy Greens (ADEG), Original Flavor, Net Wt 11.36 oz (322g), UPC Code 893320002096

NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress.

Recall #
F-1005-2016
Affected scope
563,499 units
Initiated
March 11, 2016
Verify with FDA Food →

The recall

Naturmed Inc DBA Institute for Vibrant Living issued this moderate-severity FDA Food recall — NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due t….

Moderate
severity level
563K units
affected scope
Class II
classification
April 6, 2016
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1005-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-1005-2016) was formally reported on April 6, 2016, with the manufacturer initiating the action on March 11, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Naturmed Inc DBA Institute for Vibrant Living is listed as the recalling firm, operating out of Camp Verde, AZ. Federal records list the affected scope as 563,499 units, a scale large enough to require multi-state distribution tracking.

The documented reason for this recall is: NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress. Distribution data in the federal record shows the product reached: US. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 4 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Dietary Supplements recalls over time

Where this recall sits in its category — 663 dietary supplements recalls on record

-50050100150 2008201220152018202120242026 3

Where this recall sits in the database

Severity2119858883High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified moderate severity.

Severity

Moderate

Affected scope

563,499 units

Related Recalls

6

4 from same agency

Product description

All Day Energy Greens (ADEG), Original Flavor, Net Wt 11.36 oz (322g), UPC Code 893320002096

Reason for recall

NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number F-1005-2016
Date reported April 6, 2016
Date initiated March 11, 2016
Recalling firm Naturmed Inc DBA Institute for Vibrant Living
Firm location Camp Verde, AZ
Affected scope 563,499 units
Distribution US

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

563,499 units units affected — multi-state distribution scale.

Regional (<10K units)
Multi-state (10K – 100K units)
Large-scale (100K – 1M units) ✓ This recall
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

Frequently Asked Questions

What product was recalled?
All Day Energy Greens (ADEG), Original Flavor, Net Wt 11.36 oz (322g), UPC Code 893320002096. Recalled by Naturmed Inc DBA Institute for Vibrant Living. Units affected: 563,499 units.
Why was this product recalled?
NatureMed Inc. dba Institute for Vibrant Living is recalling All Day Energy Greens powdered green drink due to some reported cases of gastrointestinal distress.
Which agency issued this recall?
This recall was issued by the FDA Food on April 6, 2016. Severity: Moderate. Recall number: F-1005-2016.
Where was the recalled product distributed?
Distribution: US.
How do I check if my product is affected by a recall?
Check the product description and recall number (F-1005-2016) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

Compare this recall with Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Di… →

Data Sources

Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported April 6, 2016.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)

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.

Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).