FDAClass IIRecall started July 2, 2026

Sweet Sensi Elevated Edibles Hybrid Gum Drops – Passion Guava Kush 140 mg THC Recall

Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product is packaged in sealable & flexible gold, purple and black metallic plastic mylar pouch and is sold in two sizes: 1) Net wt. Approx. 2.1oz (60g) 10 count and 2) Net wt. 6.3oz (180g) 30 count. Batch #1811, Manufactured by Sweet Sensi Austin, TX 78734. UPC 850043378020

What is the FDA recall status?

The FDA record lists this recall as ongoing. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions and check the agency notice or firm for current guidance.

How FDA enforcement data reports status

Why was Sweet Sensi Hybrid Gum Drops – Passion Guava Kush recalled?

Staphylococcus aureus detected in product.

What should I do if I have this product?

Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.

Which lot codes, UPCs or models are affected?

Batch # 1811 UPC 850043378020

Agency record number
H-0020-2027
Product
Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product is packaged in sealable & flexible gold, purple and black metallic plastic mylar pouch and is sold in two sizes: 1) Net wt. Approx. 2.1oz (60g) 10 count and 2) Net wt. 6.3oz (180g) 30 count. Batch #1811, Manufactured by Sweet Sensi Austin, TX 78734. UPC 850043378020
Recalling firm
SWEET SENSI
Quantity
6,176 (10ct pouches), 4,359 (30ct pouches)
Distribution
Nationwide
Recall started
July 2, 2026
Report date
October 14, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (food)
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