Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product is packaged in sealable & flexibl
Summary
The FDA issued a Class II for Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. P by SWEET SENSI. Reason: Staphylococcus aureus detected in product..
Details
Source
Food Recall
External ID
H-0020-2027
Action Date
2026-10-14
Status
Ongoing
Category
food
Product Description
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
Lot/Code Info: Batch # 1811 UPC 850043378020
Quantity Affected: 6,176 (10ct pouches), 4,359 (30ct pouches)
Reason for Recall
Staphylococcus aureus detected in product.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-02
Company
Austin, TX
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 35 food recalls issued in the same week, part of 92 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (SWEET SENSI) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SWEET SENSI have FDA actions?
This is the only FDA action we have on record for SWEET SENSI in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0020-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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