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Stop using now Food recall · FDA · Published July 2, 2026

Sweet Sensi Gum Drops Recalled for Staphylococcus aureus

Sweet Sensi recalls Passion Guava Kush gum drops due to Staphylococcus aureus contamination. Check your batch #1811 immediately.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-0020-2027FoodSweet Sensi ›
✎ GovInfoNow plain-language explainer

Sweet Sensi is recalling Elevated Edibles Hybrid Gum Drops in the Passion Guava Kush flavor because Staphylococcus aureus was detected in the product. The affected items are packaged in sealable metallic mylar pouches and were distributed nationwide. No specific remedy or return instructions are currently listed in the record. Read more at govinfonow.com/recall/1614512-sweet-sensi-recalls-sweet-sensi-elevated-edibles-hybrid-gum-drops.

Source Summary by GovInfoNow · govinfonow.com/recall/1614512-sweet-sensi-recalls-sweet-sensi-elevated-edibles-hybrid-gum-drops · Updated October 21, 2026 · Official notice: FDA #H-0020-2027

Cite this page

“Sweet Sensi Gum Drops Recalled for Staphylococcus aureus.” GovInfoNow, updated October 21, 2026. https://govinfonow.com/recall/1614512-sweet-sensi-recalls-sweet-sensi-elevated-edibles-hybrid-gum-drops. Based on FDA recall #H-0020-2027.

Sweet Sensi recalled its Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC due to Staphylococcus aureus contamination, according to the FDA. The agency announced the voluntary recall on July 2, 2026.

How to tell if you have it

  • Brand: Sweet Sensi
  • Product: Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC
  • Packaging: sealable & flexible gold, purple and black metallic plastic mylar pouch
  • Sizes: Net wt. Approx. 2.1oz (60g) 10 count; Net wt. 6.3oz (180g) 30 count
  • Batch #: 1811
  • UPC: 850043378020

The hazard

Staphylococcus aureus was detected in the product, according to the FDA.

Context

GovInfoNow's records show other recent recalls of similar products include Taylor Fresh Foods Spicy Guacamole Recall: Salmonella Contamination Risk (2026-08-07) and Spring & Mulberry Sea Salt Date-Sweetened Chocolate Recall: Potential Salmonella Contamination (2026-01-09). Additional similar recalls include the Spring & Mulberry Pecan Date-Sweetened Chocolate Recall: Potential Salmonella Contamination (2026-01-09).

How to tell if you have this one

Check for Sweet Sensi Elevated Edibles Hybrid Gum Drops in Passion Guava Kush flavor, packaged in gold, purple, and black metallic plastic mylar pouches. Verify if your product has Batch #1811 and UPC 850043378020. The product is available in two sizes: approximately 2.1oz (60g) 10-count packs or 6.3oz (180g) 30-count packs.

  • Brand
    Sweet Sensi
  • Product
    Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product is packaged in sealable &
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled gum drops if you have Batch #1811.

  2. Check your packaging details

    Verify that your package matches the description of gold, purple, and black metallic mylar pouches with UPC 850043378020.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 3 months after the firm started it.

1. Firm started the recall: Jul 2, 202612. FDA classified it Class II: Oct 7, 202623. Published in FDA’s Enforcement Report: Oct 14, 202634. Added to GovInfoNow: Oct 21, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-0020-2027 (July 2, 2026)
  • Plain-language summary written by qwen3.6:35b-a3b on October 21, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA