Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count Bag, Product Number MSC351450BG4
FDA Recall Z-2926-2026 · Posted 2026-08-07
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Recalling FirmMedline Industries, LP
Recall StatusOpen, Classified
Product CodeLRJ
Date Initiated2026-06-30
Product Quantity31,728
Reason for Recall
Medline Micro-Kill Bleach Germicidal Bleach 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.
Firm Action
An URGENT MEDICAL DEVICE RECALL notification letter dated 6/30/26 was sent to customers.
REQUIRED ACTION:
1.Immediately check your stock for the affected item number(s) and the affected lot number(s) listed within the recall portal. Quarantine all affected product. Upon completion of the below actions, please destroy affected product.
2.Please use the link and the information below to complete your response form. Please list the quantity of affected product you have in inventory on the form. Even if you do not have any affected product in inventory, please complete and submit the response form.
Website link: https://recalls.medline.com
Recall Reference #: R-26-104
Recall Code:
3.Your account will receive credit once the response form is submitted.
4.If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please request that customers destroy any affected product. You should include your customers quantities on your response form.
If you have any questions, contact the Recall Department at 866-359-1704 or [email protected].
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution in the states and territories of Guam, Puerto Rico.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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