PlainRecalls
FDA Drug Moderate Class II Terminated

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.

Reported: December 29, 2021 Initiated: November 8, 2021 #D-0287-2022

Product Description

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.

Reason for Recall

Defective Container: Customer complaints for leaking bottles and dispensing issues.

Details

Recalling Firm
Medline Industries Inc
Units Affected
470,555 bottles
Distribution
Nationwide in the USA, Canada, Hong Kong, and Peru
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
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.. Recalled by Medline Industries Inc. Units affected: 470,555 bottles.
Why was this product recalled?
Defective Container: Customer complaints for leaking bottles and dispensing issues.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 29, 2021. Severity: Moderate. Recall number: D-0287-2022.