Class IIOngoingVoluntary: Firm initiated
SWEET SENSI: food recall H-0020-2027
SWEET SENSI of Austin, TX recalled Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product is packaged in sealable &… Reason: Staphylococcus aureus detected in product. The FDA listed it as Class II in its Enforcement Report dated Oct 14, 2026; distribution: nationwide.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- 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
- Product quantity
- 6,176 (10ct pouches), 4,359 (30ct pouches)
- Reason for recall
- Staphylococcus aureus detected in product.
- Codes, lots and dates on the package
- Batch # 1811 UPC 850043378020
- Distribution pattern
- Nationwide
- Recalling firm
- SWEET SENSI, Austin, TX
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Letter
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jul 2, 2026 |
| Classified by the FDA | Oct 7, 2026 |
| Published in the Enforcement Report | Oct 14, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0020-2027 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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