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Class I: serious health riskTerminated

Pdx Aromatics GREEN Kratom POWDER Recall

GREEN Kratom POWDER, 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-1527-2018
Check your lot numberHow we source this data

Summary

Pdx Aromatics recalled GREEN Kratom POWDER starting Mar 9, 2018. The FDA classified it as Class I (serious health risk) and published enforcement report F-1527-2018 on Mar 28, 2018. Reason: Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom POWDER are recalled due to potential contamination with Salmonella. Status: Terminated.

Why it was recalled

Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom POWDER are recalled due to potential contamination with Salmonella.

Product description

GREEN Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The powder 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 OG Bali Powder Kraken Kratom Super Green Malaysian Kratom Powder Phytoextractum OG Bali Powder Phytoextractum Green Vein Thai Kratom Powder Phytoextractum Super Green Malaysian Kratom Powder Soul Speciosa OG Bali Powder Soul Speciosa Thai Kratom Powder (Green Vein) Soul Speciosa Super Green Malaysian Kratom Powder

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 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 Additionally, the GREEN VEIN powder products EXCEPT OG Bali Powder listed below have any of the following LOT codes: LOT 20170918 LOT 20170919 LOT 20170920 LOT 20170921 LOT 20170922 LOT 20170923 LOT 20170924 LOT 20170925 LOT 20170926 LOT 20170927 LOT 20170928 LOT 20170929 LOT 20170930 LOT 20171001 LOT 20171002 LOT 20171003 LOT 20171004 LOT 20171005 LOT 20171006 LOT 20171007 LOT 20171008 LOT 20171009 LOT 20171010 LOT 20171011 LOT 20171012 LOT 20171013 LOT 20171014 LOT 20171015 LOT 20171016 LOT 20171017 LOT 20171018 LOT 20171019 LOT 20171020 LOT 20171021 LOT 20171022 LOT 20171023 LOT 20171024 LOT 20171025 LOT 20171026 LOT 20171027 LOT 20171028 LOT 20171029 LOT 20171030 LOT 20171031 LOT 20171101

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-1527-2018
Classification
Class I
Status
Terminated
Recall initiated
Mar 9, 2018
FDA report date
Mar 28, 2018
Quantity
20,546 pkgs.
Recall type
Voluntary: Firm initiated
Recalling firm
Pdx Aromatics

Original FDA data

Every field from FDA enforcement report F-1527-2018, 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 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 Additionally, the GREEN VEIN powder products EXCEPT OG Bali Powder listed below have any of the following LOT codes: LOT 20170918 LOT 20170919 LOT 20170920 LOT 20170921 LOT 20170922 LOT 20170923 LOT 20170924 LOT 20170925 LOT 20170926 LOT 20170927 LOT 20170928 LOT 20170929 LOT 20170930 LOT 20171001 LOT 20171002 LOT 20171003 LOT 20171004 LOT 20171005 LOT 20171006 LOT 20171007 LOT 20171008 LOT 20171009 LOT 20171010 LOT 20171011 LOT 20171012 LOT 20171013 LOT 20171014 LOT 20171015 LOT 20171016 LOT 20171017 LOT 20171018 LOT 20171019 LOT 20171020 LOT 20171021 LOT 20171022 LOT 20171023 LOT 20171024 LOT 20171025 LOT 20171026 LOT 20171027 LOT 20171028 LOT 20171029 LOT 20171030 LOT 20171031 LOT 20171101
Postal code
97227-1708
Report date
Mar 28, 2018
Product type
Food
Recall number
F-1527-2018
Classification
Class I
Recalling firm
Pdx Aromatics
Product quantity
20,546 pkgs.
Termination date
Sep 13, 2018
Reason for recall
Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom POWDER are recalled due to potential contamination with Salmonella.
Voluntary / mandated
Voluntary: Firm initiated
Product description
GREEN Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The powder 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 OG Bali Powder Kraken Kratom Super Green Malaysian Kratom Powder Phytoextractum OG Bali Powder Phytoextractum Green Vein Thai Kratom Powder Phytoextractum Super Green Malaysian Kratom Powder Soul Speciosa OG Bali Powder Soul Speciosa Thai Kratom Powder (Green Vein) Soul Speciosa Super Green Malaysian Kratom Powder
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-1527-2018, published Mar 28, 2018. View the source record (openFDA) · FDA enforcement reports

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

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