CLASS II Food recall · Reported 26 Sep 2012 · FDA Enforcement Report
Dietary supplement recalled by GMP Laboratories of America
GMP Laboratories of America is recalling Dietary supplement, distributed nationwide in the US. The recall was initiated on 8 Dec 2009 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-2297-2012
- FDA event ID
- 62786
- Recalling firm
- GMP Laboratories of America, Anaheim, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 8 Dec 2009
- FDA classified
- 14 Sep 2012
- Reported
- 26 Sep 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Product category
- Herbal Supplements
Timeline
| 8 Dec 2009 | Recall initiated by company | |
| 14 Sep 2012 | Classified by FDA | +1011 days |
| 26 Sep 2012 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
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***".
Where it was distributed
US States nationwide.
Questions about this recall
Is Dietary supplement recalled?
Yes. GMP Laboratories of America recalled Dietary supplement on 8 Dec 2009. The recall is Class II and its status is Terminated. Recall number F-2297-2012.
Why was it recalled?
The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.
Which lots are affected?
LOT 2448 BEST BY 10/12
Where was it sold?
US States nationwide.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from GMP Laboratories of America
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS III | Lithium Orotate 5;, Dietary Supplement recalledLithium Orotate | GMP Laboratories of America | Potency & Assay | CA, OK |
| Food | CLASS III | Lithium Orotate, Weyland Brain Nutrition ;, Dietary Supplement recalledLithium Orotate | GMP Laboratories of America | Potency & Assay | CA, OK |
Other Herbal Supplements recalls
All 509| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | Lacnola; Small recalled by The Hampton Grocer | The Hampton Grocer | Salmonella | Nationwide |
| Food | ANNOUNCED | Moringa Leaf Powder recalled by Foods AliveFoods Alive | Foods Alive | Salmonella | Nationwide |
| Food | CLASS II | A-L Complex Herbal Supplement May Contain Nuts recalledByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |
| Food | CLASS II | A-P Herbal Supplement May Contain Nuts recalled by Byron White FormulasByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |
| Food | CLASS II | A-fng Herbal Supplement May Contain Nuts recalledByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |