CLASS I Drug recall · Reported 9 Sep 2020 · FDA Enforcement Report
SkinGuard 24 All-Day Hand Sanitizer bottle with foam pump recalled
SG24 is recalling SkinGuard 24 All-Day Hand Sanitizer bottle with foam pump, Dist by: SG24 LLC, Bolingbroke, distributed nationwide in the US. The recall was initiated on 14 Aug 2020 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1572-2020
- FDA event ID
- 86270
- Recalling firm
- SG24, Bolingbroke, GA
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 14 Aug 2020
- FDA classified
- 11 Sep 2020
- Reported
- 9 Sep 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Hidden Drug Ingredients
- Drug class
- Hand Sanitizer
Timeline
| 14 Aug 2020 | Recall initiated by company | |
| 9 Sep 2020 | Published in enforcement report | +26 days |
| 11 Sep 2020 | Classified by FDA | +2 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed without an Approved NDA/ANDA; product labeled to contain 0.56% methanol making it an unapproved new drug
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump, Dist by: SG24 LLC, Bolingbroke, GA 31004 UPC 793573147125
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Marketed without an Approved NDA/ANDA; product labeled to contain 0.56% methanol making it an unapproved new drug
Which lots are affected?
SKU 051230024 All lots labeled to contain methanol
Where was it sold?
Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
3 other products · FDA event 86270| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand recalled by SG24 | SG24 | Hidden Drug Ingredients | Nationwide | |
| CLASS I | Skin Guard 24 All-Day Hand Sanitizer Pocket Pen Dist recalled by SG24 | SG24 | Hidden Drug Ingredients | Nationwide | |
| CLASS I | SkinGuard 24 All-Day Hand Sanitizer bottle with foam pump recalled | SG24 | Hidden Drug Ingredients | Nationwide |
More recalls from SG24
All 4| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | SkinGuard 24 All-Day Hand Sanitizer bottle with foam pump recalled | SG24 | Hidden Drug Ingredients | Nationwide |
| Drug | CLASS I | Skin Guard 24 All-Day Hand Sanitizer Pocket Pen Dist recalled by SG24 | SG24 | Hidden Drug Ingredients | Nationwide |
| Drug | CLASS I | Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand recalled by SG24 | SG24 | Hidden Drug Ingredients | Nationwide |