CLASS I Food recall · Reported 25 Apr 2018 · FDA Enforcement Report

Club 13 Kratom Maeng Da Red XS capsules recalled

Club 13 Enterprises Warehouse is recalling Club 13 Kratom Maeng Da Red XS capsules. The recall was initiated on 31 Mar 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLots # KRXS020718, KRXS030618, KRXS102417, KRXS110617, and KRXS120117.
Quantity recalled873 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1121-2018
FDA event ID
79716
Recalling firm
Club 13 Enterprises Warehouse, Saint Augustine, FL
Brand
Club
Classification
Class I
Status
Terminated
Recall initiated
31 Mar 2018
FDA classified
20 Apr 2018
Reported
25 Apr 2018
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Salmonella
Product category
Energy Drinks

Timeline

31 Mar 2018Recall initiated by company
20 Apr 2018Classified by FDA+20 days
25 Apr 2018Published in enforcement report+5 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Samples of Maeng Da red powder were tested and resulted positive for Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Club 13 Kratom Maeng Da Red XS capsules; 5, 20, 25, 40, 50 capsule bottles

Where it was distributed

U.S. consignees only.

Questions about this recall

Why was it recalled?

Samples of Maeng Da red powder were tested and resulted positive for Salmonella.

Which lots are affected?

Lots # KRXS020718, KRXS030618, KRXS102417, KRXS110617, and KRXS120117.

Where was it sold?

U.S. consignees only.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 79716

More recalls from Club 13 Enterprises Warehouse

All 3

Other Energy Drinks recalls

All 132