FDA recall D-0287-2022

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.

Reason for recall

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

Distribution

Nationwide in the USA, Canada, Hong Kong, and Peru

Key facts

Status

Terminated

Initiation date

2021-11-08

Report date

2021-12-29

Termination date

2024-08-28

Voluntary/Mandated

Voluntary: Firm initiated

Location

Northfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0287-2022