CLASS III Drug recall · Reported 31 Oct 2012 · FDA Enforcement Report
Earth Force, Ltd., Power Towels recalled by Abc Compounding Company
Abc Compounding is recalling Earth Force, Ltd., Power Towels, QS Plus Hand Sanitizing Wipes (antiseptic), 50, distributed nationwide in the US. The recall was initiated on 10 Feb 2011 and the FDA has classified it as Class III.
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-011-2013
- FDA event ID
- 63395
- Recalling firm
- Abc Compounding, Morrow, GA
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 10 Feb 2011
- FDA classified
- 22 Oct 2012
- Reported
- 31 Oct 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Drug class
- Compounded Drugs
Timeline
| 10 Feb 2011 | Recall initiated by company | |
| 22 Oct 2012 | Classified by FDA | +620 days |
| 31 Oct 2012 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Chemical Contamination: QS Plus wipes were found to be contaminated with different substance (7820, Graffiti Remover).
Product as listed by the FDA
Earth Force, Ltd., Power Towels, QS Plus Hand Sanitizing Wipes (antiseptic), 50 pre-moistened Wipes, Manufactured by: ABC Compounding Co., Inc., P.O. Box 16247, Atlanta, GA 30321.
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Chemical Contamination: QS Plus wipes were found to be contaminated with different substance (7820, Graffiti Remover).
Which lots are affected?
Lot #3220
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 III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
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.