Hand Sanitizer Foam (Medline) – Leaking Container (2021)
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
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Hand Sanitizer Foam (ethyl alcohol), 62% v/v, packaged in a) 1.5 Oz. cans, NDC 53329-970-12; b) 8 Oz. (227 g) cans, NDC 53329-970-08; and c) 16 Oz. (453 g) cans, NDC 53329-970-06; Manufactured for: Medline Industries, Inc., Northfield, IL 60093.
Brand
Medline Industries Inc
Lot Codes / Batch Numbers
Lot #: a) 32890, exp 04/2022, 33141, 33215, exp 10/2022, 33350, exp 12/2022, 33461, exp 03/2023, b) 32858, exp 02/2022, 32889, exp 03/2022, 32968, 32977, 32975, 32984, exp 06/2022, 33294, 33295, 33322, 33323, exp 12/2022, 33384, exp 01/2023, Lot 33620, exp 07/2023, c) 32728, exp 10/2021, 32859, 32889, exp 03/2022, 32985, 32988, 33004, exp 06/2022, 33339, exp 12/2022, 33501, exp 03/2023, 33502, exp 04/2023, 33621, 33622, exp 07/2023
Products Sold
Lot #: a) 32890, exp 04/2022; 33141, 33215, exp 10/2022; 33350, exp 12/2022; 33461, exp 03/2023; b) 32858, exp 02/2022; 32889, exp 03/2022; 32968, 32977, 32975, 32984, exp 06/2022; 33294, 33295, 33322, 33323, exp 12/2022; 33384, exp 01/2023; Lot 33620, exp 07/2023; c) 32728, exp 10/2021; 32859, 32889, exp 03/2022; 32985, 32988, 33004, exp 06/2022; 33339, exp 12/2022; 33501, exp 03/2023; 33502, exp 04/2023; 33621, 33622, exp 07/2023
Medline Industries Inc is recalling Hand Sanitizer Foam (ethyl alcohol), 62% v/v, packaged in a) 1.5 Oz. cans, NDC 53329-970-12; b) 8 Oz due to Defective Container: Customer complaints for leaking bottles and dispensing issues.. 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
Defective Container: Customer complaints for leaking bottles and dispensing issues.
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
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 7, 2026