Medline MSC351400ANRecalls & reported problems

Medline Industries, Inc. · WIPE,GERM,MICROKILLBLEACH,7X8,150CT · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

3 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports: 0
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 3

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

3 FDA recall records name this device's identifier, 3 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

Jun 30, 2026Class IIOpen, Classified
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.
Z-2923-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Dec 20, 2023Class IIOpen, Classified
There is stability concern for products dated with a 24-month shelf life. Product is safe and effective up to 12 months shelf life.
Z-1180-2024 · Root cause: Process control · Recall details · FDA record ↗
Dec 29, 2021Class IIOpen, Classified
Micro-Kill Bleach Wipes contain out of specification (low) levels of Sodium Hypochlorite.
Z-0696-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Device details

UDI-DI	`10888277652514`
Brand	Medline
Model	MSC351400AN
Company	Medline Industries, Inc.
Product code	LRJ · Disinfectant, medical devices
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	—
Single use	Yes
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jun 14, 2024

Device type (GMDN): Medical device cleaning/disinfection wipe

A moist, pre-treated fabric intended to be used to wipe the surface of medical devices and equipment to clean and/or destroy harmful microorganisms or inhibit their activity. The fabric is impregnated with a solution that may include a detergent(s) for cleaning surfaces and/or a disinfectant agent(s) or a precursor compound that forms a disinfectant agent when activated (e.g., by a separate solution). This is a single-use device.

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All Disinfectant, medical devices devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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