CLASS II Drug recall · Reported 14 Nov 2018 · FDA Enforcement Report
deb stoko, Refresh AntiBac FOAM (benzalkonium chloride) recalled
S.C. Johnson Professional is recalling deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 13% cartridge, distributed in North Carolina. The recall was initiated on 26 Oct 2018 and the FDA has classified it as Class II.
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-0220-2019
- FDA event ID
- 81453
- Recalling firm
- S.C. Johnson Professional, Charlotte, NC
- Brand
- Refresh Antibac Foam
- Manufacturer
- SC Johnson Professional USA Inc.
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 26 Oct 2018
- FDA classified
- 6 Nov 2018
- Reported
- 14 Nov 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Manufacturing (CGMP) Deviations
Timeline
| 26 Oct 2018 | Recall initiated by company | |
| 6 Nov 2018 | Classified by FDA | +11 days |
| 14 Nov 2018 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations: Product was released to market prior to microbiological testing.
Product as listed by the FDA
deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 0.13%, 1 L (33.8 fl. oz.) cartridge packaged in 8 cartridges per case, Made in the USA, Deb USA, Inc., Charlotte, NC 28217, NDC 11084-010-27.
Where it was distributed
NC
Questions about this recall
Is deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 13% cartridge recalled?
Yes. S.C. Johnson Professional recalled deb stoko, Refresh AntiBac FOAM (benzalkonium chloride), 13% cartridge on 26 Oct 2018. The recall is Class II and its status is Terminated. Recall number D-0220-2019.
Why was it recalled?
CGMP Deviations: Product was released to market prior to microbiological testing.
Which lots are affected?
Lot 9131
Where was it sold?
NC
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 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 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from S.C. Johnson Professional
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Alcohol Free Foaming Hand Sanitizer (benzalkonium chloride) recalled | S.C. Johnson Professional | Manufacturing (CGMP) Deviations | NC |
Other Benzalkonium Chloride recalls
All 21| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Trifluent Pharma Tridergel Wound Care Gel recalled by Blaine LabsTridergel | Blaine Labs | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Revitaderm Wound Care, First Aid Antiseptic Gel recalled by Blaine LabsRevitaderm Wound Care | Blaine Labs | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Cleansing Towelette (Benzalkonium Chloride 13%) recalled by Acme UnitedMed Nap Cleansing Towelette | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Green Guard Antiseptic Wipes (Benzalkonium Chloride 13%) recalledGreen Guard Antiseptic Wipes | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Dukal BZK Antiseptic Towelette (Benzalkonium Chloride 13%) recalledBzk Towelette | Acme United | Manufacturing (CGMP) Deviations | Nationwide |