Medline Bleach Wipes Recalled for Reduced Disinfection Effectiveness
Medline is recalling bleach wipes that may lose potency before expiration, potentially allowing pathogens to survive.
The agency’s classification
FDA (Devices): Class II
Class II is 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.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product where the hazard is the potential survival of pathogenic microorganisms due to reduced disinfection effectiveness, but no injuries or illnesses have been reported.
Plain-English summary
Medline Industries, LP is recalling 1,244 units of Medline Micro-Kill Bleach Germicidal Bleach Wipes (12" x 12", 110 Count, Product Number MSC351450AN). The affected units were distributed nationwide in the United States, including the territories of Guam and Puerto Rico. The recall covers all lots produced between October 27, 2025, and November 19, 2025.
The recall is due to a potential reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life. This reduction may compromise the effectiveness of disinfection, potentially allowing for the survival and persistence of pathogenic microorganisms.
Consumers and healthcare facilities should stop using the affected wipes and contact Medline Industries, LP for instructions on return or replacement.
The recalled product
- Product
- Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count, Product Number MSC351450AN
- Manufacturer
- Medline Industries, LP
- Affected units
- 1,244
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- UDI-DI (each) 80080196314521
- UDI-DI (case) 10080196314522
- Lot Numbers: All lots produced between 10/27/2025 and 11/19/2025
Distribution
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