Fresh Recalls

FDAClass II · Food · Recall H-0020-2027 · Recalled October 14, 2026

Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC recall — SWEET SENSI

Agency report date: October 14, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC
Company / brand
SWEET SENSI
Lot / serial / date codes
Batch # 1811 UPC 850043378020
Distribution
Nationwide
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Staphylococcus aureus detected in product.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC recall status

3. Open the official notice or contact

Official recall ID
H-0020-2027
Brand
All SWEET SENSI recalls
Classification
Class II
Units affected
6,176 (10ct pouches), 4,359 (30ct pouches)
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Austin, TX, United States
Firm address
15004 Cavalier Canyon Dr Unit A, N/A, 78734-3600

Identifying details (verbatim from the notice)

Product codes / lots
Batch # 1811 UPC 850043378020
Distribution
Nationwide
Firm notified the public via
Letter
FDA event ID
99442
Recall initiated
July 2, 2026
FDA classified
October 7, 2026
FDA report date
October 14, 2026

Other food recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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