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Majopa Industries Corporation recall — Label reads in part as: "GRAVIOLA EXTRACT***1 FL Oz (30 ml)***…
FDA (enforcement) · September 30, 2015 · Class I
- Majopa Industries Corporation recalled Label reads in part as: "GRAVIOLA EXTRACT***1 FL Oz (30 ml)*** ORIGINAL… — an FDA enforcement event posted , classified Class I, covering 1 product entry.
- FDA-stated reason: Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the FD&C Act.
- Details as of ; the linked official notice is authoritative for lot codes, VINs, and remedies.
- Agency
- FDA
- Posted
- Initiated
- Classification
- Class I
- Status
- Terminated
- Recalling firm
- Majopa Industries Corporation
- Source ID
- 71918
FDA Enforcement Report search →
Product entries (1)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| F-3245-2015 | Label reads in part as: "GRAVIOLA EXTRACT***1 FL Oz (30 ml)*** ORIGINAL FORMULA***Manufactured by: Majopa Industries Corp.*** PRODUCT OF PUERTO RICO,USA". … | 02/2020 | Puerto Rico only |
FDA enforcement entries have no per-recall public URL — verify via the FDA Enforcement Report search using the firm name or a recall number above.
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