Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 8, 2009 (17 years ago)

Dietary supplement Product is labeled as recall

Recalled by GMP Laboratories of America Inc · Anaheim, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

See the recall's own reason text for the specifics. All other reasons recalls.

What 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***".

Quantity: 1027 boxes

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

LOT 2448 BEST BY 10/12

Where it was sold

Nationwide.

FDA's distribution note: US States nationwide.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
GMP Laboratories of America Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 8, 2009
In FDA report of
Sep 26, 2012
Terminated
Sep 14, 2012
FDA recall number
F-2297-2012 · event 62786
Official record
FDA enforcement report search

Other recalls by GMP Laboratories of America Inc

Class III · Low risk Terminated Other

Lithium Orotate Weyland Brain Nutrition

Reason Downstream recall of a dietary supplement ingredient that was manufactured out of specification.

GMP Laboratories of America Inc CA, OK H-0448-2025
Class III · Low risk Terminated Other

Lithium Orotate 2.5

Reason Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.

GMP Laboratories of America Inc CA, OK H-0447-2025

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