Dietary supplement — Class II food recall F-2297-2012
Terminated recall by GMP Laboratories of America Inc, reported 2012-09-26, distributed nationwide. The firm recalled because the product lot contained mispackaged product wherein some capsules were missing fro
| Recall number | F-2297-2012 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GMP Laboratories of America Inc, Anaheim, CA, United States |
| Recall initiated | 2009-12-08 |
| Classified | 2012-09-14 |
| Reported by FDA | 2012-09-26 |
| Terminated | 2012-09-14 |
| Distributed | Nationwide (US) |
| Quantity | 1,027 boxes |
| Lot numbers | 10/12, 2448 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-2297-2012. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.