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Class I: serious health riskTerminated

Pdx Aromatics RED Kratom CAPSULES Recall

RED Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Spe…

Pdx Aromatics · Portland, OR

Risk level
Class I
Reported by FDA
Mar 28, 2018
Recall ID
F-1528-2018
Check your lot numberHow we source this data

Summary

Pdx Aromatics recalled RED Kratom CAPSULES starting Mar 9, 2018. The FDA classified it as Class I (serious health risk) and published enforcement report F-1528-2018 on Mar 28, 2018. Reason: Kraken Kratom, Phytoextractum, and Soul Speciosa RED VEin Kratom Capsule are recalled due to potential contamination with Salmonella. Status: Terminated.

Why it was recalled

Kraken Kratom, Phytoextractum, and Soul Speciosa RED VEin Kratom Capsule are recalled due to potential contamination with Salmonella.

Product description

RED Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The capsules are packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces). The varieties under each brand include: Kraken Kratom Red Maeng Da Capsules Phytoextractum Red Maeng Da Thai Capsules Soul Speciosa Red Maeng Da Capsules

Lot numbers, UPCs & expiration codes

The lot code represents the day packaged. The first four digits are the year, followed by two digits for the month, followed by two digits for the day. LOT 20171201 LOT 20171202 LOT 20171203 LOT 20171204 LOT 20171205 LOT 20171206 LOT 20171207 LOT 20171208 LOT 20171209 LOT 20171210 LOT 20171211 LOT 20171212 LOT 20171213 LOT 20171214 LOT 20171215 LOT 20171216 LOT 20171217 LOT 20171218 LOT 20171219 LOT 20171220 LOT 20171221 LOT 20171222 LOT 20171223 LOT 20171224 LOT 20171225 LOT 20171226 LOT 20171227 LOT 20171228 LOT 20171229 LOT 20171230 LOT 20171231 LOT 20180101 LOT 20180102 LOT 20180103 LOT 20180104 LOT 20180105 LOT 20180106 LOT 20180107 LOT 20180108 LOT 20180109 LOT 20180110 LOT 20180111 LOT 20180112 LOT 20180113 LOT 20180114 LOT 20180115 LOT 20180116 LOT 20180117 LOT 20180118 LOT 20180119 LOT 20180120 LOT 20180121 LOT 20180122 LOT 20180122 LOT 20180124 LOT 20180125 LOT 20180126 LOT 20180127 LOT 20180128 LOT 20180129 LOT 20180130 LOT 20180131 LOT 20180201 LOT 20180202 LOT 20180203 LOT 20180204 LOT 20180205 LOT 20180206 LOT 20180207 LOT 20180208 LOT 20180209 LOT 20180210 LOT 20180211 LOT 20180212 LOT 20180213 LOT 20180214 LOT 20180215 LOT 20180216 LOT 20180217 LOT 20180218 LOT 20180219 LOT 20180220 LOT 20180221 LOT 20180222 LOT 20180223 LOT 20180224 LOT 20180225 LOT 20180226 LOT 20180227 LOT 20180228 LOT 20180301 LOT 20180302 LOT 20180303 LOT 20180304 LOT 20180305 LOT 20180306 LOT 20180307 LOT 20180308

Where it was sold

distributed throughout the U.S.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1528-2018
Classification
Class I
Status
Terminated
Recall initiated
Mar 9, 2018
FDA report date
Mar 28, 2018
Quantity
10,210 packages
Recall type
Voluntary: Firm initiated
Recalling firm
Pdx Aromatics

Original FDA data

Every field from FDA enforcement report F-1528-2018, exactly as published.

Show all FDA fields
City
Portland
State
OR
Status
Terminated
Country
United States
Event ID
79480
Address
2170 N Lewis Ave Ste 250
Code information
The lot code represents the day packaged. The first four digits are the year, followed by two digits for the month, followed by two digits for the day. LOT 20171201 LOT 20171202 LOT 20171203 LOT 20171204 LOT 20171205 LOT 20171206 LOT 20171207 LOT 20171208 LOT 20171209 LOT 20171210 LOT 20171211 LOT 20171212 LOT 20171213 LOT 20171214 LOT 20171215 LOT 20171216 LOT 20171217 LOT 20171218 LOT 20171219 LOT 20171220 LOT 20171221 LOT 20171222 LOT 20171223 LOT 20171224 LOT 20171225 LOT 20171226 LOT 20171227 LOT 20171228 LOT 20171229 LOT 20171230 LOT 20171231 LOT 20180101 LOT 20180102 LOT 20180103 LOT 20180104 LOT 20180105 LOT 20180106 LOT 20180107 LOT 20180108 LOT 20180109 LOT 20180110 LOT 20180111 LOT 20180112 LOT 20180113 LOT 20180114 LOT 20180115 LOT 20180116 LOT 20180117 LOT 20180118 LOT 20180119 LOT 20180120 LOT 20180121 LOT 20180122 LOT 20180122 LOT 20180124 LOT 20180125 LOT 20180126 LOT 20180127 LOT 20180128 LOT 20180129 LOT 20180130 LOT 20180131 LOT 20180201 LOT 20180202 LOT 20180203 LOT 20180204 LOT 20180205 LOT 20180206 LOT 20180207 LOT 20180208 LOT 20180209 LOT 20180210 LOT 20180211 LOT 20180212 LOT 20180213 LOT 20180214 LOT 20180215 LOT 20180216 LOT 20180217 LOT 20180218 LOT 20180219 LOT 20180220 LOT 20180221 LOT 20180222 LOT 20180223 LOT 20180224 LOT 20180225 LOT 20180226 LOT 20180227 LOT 20180228 LOT 20180301 LOT 20180302 LOT 20180303 LOT 20180304 LOT 20180305 LOT 20180306 LOT 20180307 LOT 20180308
Postal code
97227-1708
Report date
Mar 28, 2018
Product type
Food
Recall number
F-1528-2018
Classification
Class I
Recalling firm
Pdx Aromatics
Product quantity
10,210 packages
Termination date
Sep 13, 2018
Reason for recall
Kraken Kratom, Phytoextractum, and Soul Speciosa RED VEin Kratom Capsule are recalled due to potential contamination with Salmonella.
Voluntary / mandated
Voluntary: Firm initiated
Product description
RED Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The capsules are packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces). The varieties under each brand include: Kraken Kratom Red Maeng Da Capsules Phytoextractum Red Maeng Da Thai Capsules Soul Speciosa Red Maeng Da Capsules
Distribution pattern
distributed throughout the U.S.
Recall initiation date
Mar 9, 2018
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jun 4, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1528-2018, published Mar 28, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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