CLASS II ONGOING Food recall · Reported 14 Oct 2026 · FDA Enforcement Report

Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC recalled

Sweet Sensi is recalling Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC, distributed nationwide in the US. The recall was initiated on 2 Jul 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBatch # 1811 UPC 850043378020
Quantity recalled6,176 (10ct pouches), 4,359 (30ct pouches)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0020-2027
FDA event ID
99442
Recalling firm
Sweet Sensi, Austin, TX
Classification
Class II
Status
Ongoing
Recall initiated
2 Jul 2026
FDA classified
7 Oct 2026
Reported
14 Oct 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Product category
Other

Timeline

2 Jul 2026Recall initiated by company
7 Oct 2026Classified by FDA+97 days
14 Oct 2026Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Staphylococcus aureus detected in product.

Product as listed by the FDA

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

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Staphylococcus aureus detected in product.

Which lots are affected?

Batch # 1811 UPC 850043378020

Where was it sold?

Nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Oct 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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