HAND-I-SAN — Class II drug recall D-0640-2024
Completed recall by Zeco LLC, reported 2024-08-28, distributed nationwide. CGMP Deviations: sterile water not used for production
| Recall number | D-0640-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zeco LLC, Chattanooga, TN, United States |
| Recall initiated | 2024-08-05 |
| Classified | 2024-08-20 |
| Reported by FDA | 2024-08-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Reason classes | sterility, cgmp |
| Expiration dates | 2024-07-27, 2024-08-09, 2024-08-15, 2024-09-23, 2024-09-29, 2024-11-17, 2024-12-20, 2025-01-23, 2025-02-21, 2025-03-03, 2025-03-10, 2025-03-15, 2025-03-30, 2025-04-10, 2025-04-21, 2025-05-11, 2025-05-17, 2025-06-06, 2025-07-17, 2025-08-10, 2025-08-24, 2025-10-02, 2025-10-13, 2025-11-01, 2025-12-05 and 6 more |
Product
HAND-I-SAN, No-Rinse Hand Sanitizer (75% Isopropyl Alcohol), packaged in a) 3.78L (1-gallon jug packaged in a case of 4x1 gallon jugs), b) 18.92L (5-gallon pail), c) 208.19L (55-gallon drum), and d) 1040.98L (275-gallon tote), ZEE Company 3401 Cummings Road, Chattanooga, TN, 37419, NDC 86161-210
Reason for recall
CGMP Deviations: sterile water not used for production
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-0640-2024. 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.