Class IITerminated in FDA datasetRecall initiated Dec 8, 2009

Dietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley living…

Recalling firm: GMP Laboratories of America Inc

Why it was recalled

The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged 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: Sep 14, 2012.

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

ProductDietary 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***".

FDA code information

LOT 2448 BEST BY 10/12

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Full FDA record and distribution details

Original 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***".

Original FDA recall reason

The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.

Recall details

Recall number
F-2297-2012
Event ID
62786
FDA status
Terminated
Initiated
Dec 8, 2009
Reported
Sep 26, 2012
Classified
Sep 14, 2012
Terminated
Sep 14, 2012
Quantity
1027 boxes
Location
Anaheim, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

US States nationwide.

FDA source record · F-2297-2012

Data updated September 16, 2026. View official FDA data ↗

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