Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported September 26, 2012
Dietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley living herbal formulas***HERBAL SUPPLEMENT 15 INDIVIDUAL PACKETS 4 VEGAN CAPSULES PER PACKET (2-368mg/2-584mg Each)***DISTRIBUTED EXCLUSIVELY BY: Living Herbal Pharmacy, LLC PO Box 56-2410, Miami, FL 33256-2410***".
The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.
Gmp Laboratories of America Inc recalled Dietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley li… - a moderate-severity action.
Dietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley li… was recalled by Gmp Laboratories of America Inc in September 26, 2012. Reason: The firm recalled because the product lot contained mispackaged product wherein some capsules were missing fr…. Check the official notice for the remedy. Verify recall #F-2297-2012 with the FDA Food before acting.
The recall
Gmp Laboratories of America Inc issued this moderate-severity FDA Food recall-The firm recalled because the product lot contained mispackaged product wherein some capsules were missing fr….
- Moderate
- severity level
- Class II
- classification
- September 26, 2012
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-2297-2012 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-2297-2012) was formally reported on September 26, 2012, with the manufacturer initiating the action on December 8, 2009. It is classified under Moderate severity (Class II), with a current status of Terminated. Gmp Laboratories of America Inc is listed as the recalling firm, operating out of Anaheim, CA. Federal records list the affected scope as 1027 boxes.
The documented reason for this recall is: The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product. Distribution data in the federal record shows the product reached: US States nationwide.. 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, 6 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 - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1027 boxes
Related Recalls
6
6 from same agency
Product description
Dietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley living herbal formulas***HERBAL SUPPLEMENT 15 INDIVIDUAL PACKETS 4 VEGAN CAPSULES PER PACKET (2-368mg/2-584mg Each)***DISTRIBUTED EXCLUSIVELY BY: Living Herbal Pharmacy, LLC PO Box 56-2410, Miami, FL 33256-2410***".
Reason for recall
The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-2297-2012 |
| Date reported | September 26, 2012 |
| Date initiated | December 8, 2009 |
| Recalling firm | Gmp Laboratories of America Inc |
| Firm location | Anaheim, CA |
| Affected scope | 1027 boxes |
| Distribution | US States nationwide. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-2297-2012) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Dietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley living herbal formulas***HERBAL SUPPLEMENT 15 INDIVIDUAL PACKETS 4 VEGAN CAPSULES PER PACKET (2-368mg/2-584mg Each)***DISTRIBUTED EXCLUSIVELY BY: Living Herbal Pharmacy, LLC PO Box 56-2410, Miami, FL 33256-2410***".. Recalled by Gmp Laboratories of America Inc. Units affected: 1027 boxes.
Why was this product recalled? ▼
The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on September 26, 2012. Severity: Moderate. Recall number: F-2297-2012.
Where was the recalled product distributed? ▼
Distribution: US States nationwide..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-2297-2012) 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.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported September 26, 2012. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.