Hand Sanitizer (Zeco) – Production Water Issue (2024)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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
Brand
Zeco LLC
Lot Codes / Batch Numbers
Lot #: a) 41320, Exp. Date 7/27/2024, 41020, Exp. Date 8/9/2024, BC06614, Exp. Date 8/15/2024, BCT07768, Exp. Date 9/23/2024, BCT09410, Exp. Date 11/17/2024, CCT02139, Exp. Date 3/10/2025, CCT01561, Exp. Date 3/15/2025, CCT02953, Exp. Date 4/10/2025, CCT02346, Exp. Date 4/21/2025, CCT03654, Exp. Date 5/11/2025, CCT04010, Exp. Date 5/17/2025, CCT07274, Exp. Date 8/24/2025, CCT09516, Exp. Date 11/1/2025, CCT10500, Exp. Date 12/5/2025, DCT01157, Exp. Date 2/1/2026, DCT01586, Exp. Date 2/14/2026, DCT03947, Exp. Date 4/30/2026, DCT04406, Exp. Date 5/24/2026, CCT01651, Exp. Date 2/21/2025 b) CCT03654, Exp. Date 5/11/2025 c) BCT07768, Exp. Date 9/23/2024, BCT07975, Exp. Date 9/29/2024, BCT09410, Exp. Date 11/17/2024, BCT10246, Exp. Date 12/20/2024, CCT00705, Exp. Date 1/23/2025, CCT01952, Exp. Date 3/3/2025, CCT02139, Exp. Date 3/10/2025, CCT02689, Exp. Date 3/30/2025, CCT02346, Exp. Date 4/21/2025, CCT03654, Exp. Date 5/11/2025, CCT04010, Exp. Date 5/17/2025, CCT04630, Exp. Date 6/6/2025, CCT05946, Exp. Date 7/17/2025, CCT06785, Exp. Date 8/10/2025, CCT07274, Exp. Date 8/24/2025, CCT08515, Exp. Date 10/2/2025, CCT08936, Exp. Date 10/13/2025, CCT09516, Exp. Date 11/1/2025, CCT10888, Exp. Date 12/18/2025, DCT01157, Exp. Date 2/1/2026, DCT01586, Exp. Date 2/14/2026, DCT02902, Exp. Date 3/27/2026, DCT03947, Exp. Date 4/30/2026, CCT01952, Exp. Date 3/3/2025, d) BC06614, Exp. Date 8/15/2024, CCT00705, Exp. Date 1/23/2025, CCT06785, Exp. Date 8/10/2025, CCT10500, Exp. Date 12/5/2025, DCT01586, Exp. Date 2/14/2026
Products Sold
Lot #: a) 41320, Exp. Date 7/27/2024; 41020, Exp. Date 8/9/2024; BC06614, Exp. Date 8/15/2024; BCT07768, Exp. Date 9/23/2024; BCT09410, Exp. Date 11/17/2024; CCT02139, Exp. Date 3/10/2025; CCT01561, Exp. Date 3/15/2025; CCT02953, Exp. Date 4/10/2025; CCT02346, Exp. Date 4/21/2025; CCT03654, Exp. Date 5/11/2025; CCT04010, Exp. Date 5/17/2025; CCT07274, Exp. Date 8/24/2025; CCT09516, Exp. Date 11/1/2025; CCT10500, Exp. Date 12/5/2025; DCT01157, Exp. Date 2/1/2026; DCT01586, Exp. Date 2/14/2026; DCT03947, Exp. Date 4/30/2026; DCT04406, Exp. Date 5/24/2026; CCT01651, Exp. Date 2/21/2025 b) CCT03654, Exp. Date 5/11/2025 c) BCT07768, Exp. Date 9/23/2024; BCT07975, Exp. Date 9/29/2024; BCT09410, Exp. Date 11/17/2024; BCT10246, Exp. Date 12/20/2024; CCT00705, Exp. Date 1/23/2025; CCT01952, Exp. Date 3/3/2025; CCT02139, Exp. Date 3/10/2025; CCT02689, Exp. Date 3/30/2025; CCT02346, Exp. Date 4/21/2025; CCT03654, Exp. Date 5/11/2025; CCT04010, Exp. Date 5/17/2025; CCT04630, Exp. Date 6/6/2025; CCT05946, Exp. Date 7/17/2025; CCT06785, Exp. Date 8/10/2025; CCT07274, Exp. Date 8/24/2025; CCT08515, Exp. Date 10/2/2025; CCT08936, Exp. Date 10/13/2025; CCT09516, Exp. Date 11/1/2025; CCT10888, Exp. Date 12/18/2025; DCT01157, Exp. Date 2/1/2026; DCT01586, Exp. Date 2/14/2026; DCT02902, Exp. Date 3/27/2026; DCT03947, Exp. Date 4/30/2026; CCT01952, Exp. Date 3/3/2025; d) BC06614, Exp. Date 8/15/2024; CCT00705, Exp. Date 1/23/2025; CCT06785, Exp. Date 8/10/2025; CCT10500, Exp. Date 12/5/2025; DCT01586, Exp. Date 2/14/2026
Zeco LLC is recalling HAND-I-SAN, No-Rinse Hand Sanitizer (75% Isopropyl Alcohol), packaged in a) 3.78L (1-gallon jug pac due to CGMP Deviations: sterile water not used for production. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA drug enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
CGMP Deviations: sterile water not used for production
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm, their healthcare provider, or return it to the place of purchase.
Verify this information on the official source
This page aggregates publicly available data. Always confirm recall details directly with the U.S. Food and Drug Administration (FDA) before taking action.
View official FDA recall noticePage updated: Jan 7, 2026
Important Notice
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