Medline Industries Hand Sanitizer Foam (ethyl alcohol), 62% v/v recall — FDA D-0287-2022
Defective Container: Customer complaints for leaking bottles and dispensing issues.
Overview of recall records associated with Medline Industries Inc., including dates, categories and classifications where available.
Classification mix: Class II: 3, Class III: 1.
Defective Container: Customer complaints for leaking bottles and dispensing issues.
Superpotent Drug: Product is above specification for active ingredient, 2% Chlorhexidine Gluconate.
Microbial Contamination of Non-Sterile Product
Subpotent Drug: product not meeting the iodine assay level requirements through the labeled expiry.
This page summarizes recall records in which the official source identifies Medline Industries Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.