deb stoko — Class II drug recall D-0220-2019
Terminated recall by S.C. Johnson Professional, reported 2018-11-14, distributed in NC. CGMP Deviations: Product was released to market prior to microbiological testing.
| Recall number | D-0220-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | S.C. Johnson Professional, Charlotte, NC, United States |
| Recall initiated | 2018-10-26 |
| Classified | 2018-11-06 |
| Reported by FDA | 2018-11-14 |
| Terminated | 2020-09-08 |
| Distributed | NC |
| Quantity | 869 cases |
| Reason classes | microbial contamination, cgmp |
| NDC | 11084-0010, 11084-0010-01, 11084-0010-05, 11084-0010-12, 11084-0010-20, 11084-0010-27, 11084-0010-40, 11084-0010-55, 11084-0010-66, 11084-0010-96 |
| Lot numbers | 9131 |
Product
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.
Reason for recall
CGMP Deviations: Product was released to market prior to microbiological testing.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0220-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.