Home › Recall events › Tamarack, Inc. recall — ECLIPSE Kratom Premium Maeng Da, 40…
Tamarack, Inc. recall — ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles,…
FDA (enforcement) · April 11, 2018 · Class I
- Tamarack, Inc. recalled ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by… — an FDA enforcement event posted , classified Class I, covering 1 product entry.
- FDA-stated reason: Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella.
- 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
- Tamarack, Inc.
- Source ID
- 79565
FDA Enforcement Report search →
Product entries (1)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| F-0992-2018 | ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY | All products on market. | Distributed to retail stores in Utah. No… |
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.
Related: Salmonella recalls · Food recalls · All recall events