The Recall Desk
SevereFDA (Drugs)·D-1571-2020·Announced 2020-09-09

SkinGuard 24 Hand Sanitizer Recalled for Unapproved Methanol Content

SG24 LLC is recalling SkinGuard 24 All-Day Hand Sanitizer because it is an unapproved new drug containing methanol.

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: The agency classification is FDA Class I, which mandates a minimum severity score of 4 according to the rubric.

Plain-English summary

SG24 LLC is recalling SkinGuard 24 All-Day Hand Sanitizer, 2.67 oz. bottles with foam pumps. The product was distributed nationwide. The recall involves 9,600 bottles.

The FDA determined that the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). Additionally, the product is labeled to contain 0.56% methanol, which classifies it as an unapproved new drug.

Consumers should stop using the product and contact the recalling firm for instructions on disposal or return.

The recalled product

Product
SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump, Dist by: SG24 LLC, Bolingbroke, GA 31004 UPC 793573147103
Manufacturer
SG24 LLC
Affected units
9,600

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)

  • SKU 051220024 All lots labeled to contain methanol

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 4 recalled by SG24 LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 4 products in this recall →