FDA recall, , Moderate risk
Medline Micro-Kill Bleach Germicidal Bleach Wipes
Medline Micro-Kill Bleach Germicidal Bleach Wipes may have reduced bleach concentration before the end of their shelf life.
Summary by Recall Canary from the FDA notice
What happened
Medline Industries, LP, of Northfield, Illinois, recalled Medline Micro-Kill Bleach Germicidal Bleach Wipes because the wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life.
Reduced bleach concentration may compromise the effectiveness of disinfection, potentially allowing for the survival and persistence of pathogenic microorganisms. The recall began June 30, 2026, and was added to the FDA's Enforcement Report on August 7, 2026, with distribution nationwide in the states and territories of Guam and Puerto Rico.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your bag affected?
4 products
Affected if its UDI-DI and lot code are listed under that product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count Bag, Product Number MSC351450BG4
- UDI-DI
- 00193489015242
- 20193489015246
- Lot code
- 2025
- 2026
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count, Product Number MSC351410AN
- UDI-DI
- 10888277652521
- 20888277652528
- Lot code
- 2025
- 2026
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count, Product Number MSC351450AN
- UDI-DI
- 80080196314521
- 10080196314522
- Lot code
- 2025
Medline Micro-Kill Bleach Germicidal Bleach Wipes,7" x 8", 150 count, 150 count, Product Number MSC351400AN
- UDI-DI
- 10888277652514
- 20888277652511
- Lot code
- 2025
- 2026
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the states and territories of Guam, Puerto Rico.
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Contamination
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99432
- Recall numbers
- Z-2923-2026 to Z-2926-2026
All recalls from Medline Industries, LP
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
