Goose Creek Hand Sanitizer Spray Recalled for Chemical Contamination
Goose Creek Hand Sanitizer aloe Champagne Bubbles spray (3.38 FL. OZ.) has been recalled because it is contaminated with methanol, benzene, and acetaldehyde. Consumers should stop using the product immediately.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: This recall is classified as FDA Class I, which requires a severity score of at least 4. The product is contaminated with hazardous chemicals (methanol, benzene, and acetaldehyde) that pose serious health risks when applied to skin or inhaled during use.
Plain-English summary
Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer aloe Champagne Bubbles, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), due to chemical contamination. The product was found to be contaminated with methanol (wood alcohol), benzene, and acetaldehyde.
The affected product is identified by UPC 8 18489 01334 9 and Lot #20258. A total of 1,296 bottles were distributed nationwide in the United States.
Consumers who have purchased this product should stop using it immediately and dispose of it safely. Those with questions may contact Goose Creek at www.GooseCreekCandle.com or reach the company at 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539.
The recalled product
- Product
- Goose Creek Hand Sanitizer aloe Champagne Bubbles, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 8 18489 01334 9
- Manufacturer
- Scentsational Soaps & Candles Inc
- Category
- Drug — Hand Sanitizer
- Hazard
- methanol-contamination
- benzene-contamination
- acetaldehyde-contamination
- chemical-toxicity
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot #: 20258
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- CriticalWarfarin Tablets Recalled After Mix-Up Between 2.5 mg and 5 mg Strengths
FDA (Drugs) · 2026-07-21
- HighBeak & Skiff Alcohol Antiseptic Sanitizer recalled for acetaldehyde contamination
FDA (Drugs) · 2026-06-17
- LowPrimidone Tablets Recalled Due to Cross-Contamination with Acemetacin
FDA (Drugs) · 2026-05-27
- SevereAtomoxetine Capsules Recalled Due to Labeling Mix-Up Error
FDA (Drugs) · 2026-05-27
- SevereCIMZIA injection recalled due to lack of sterility assurance
FDA (Drugs) · 2026-05-27