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Medline Recalls Saline Wound Wash Over Sterility Concerns

Medline Industries recalled 104,608 units of sterile saline wound wash on January 5, 2026. The product may not have met the required sterility assurance level. Consumers should stop using this product immediately and follow recall instructions.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesModel Number MJSALINE7 - UDI-DI: 00708820657052 (unit)10708820657059 (case)All Lots

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
January 5, 2026
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
January 5, 2026
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Medline Industries, LP
Product type
Saline Wound Wash
Model numbers
Model Number MJSALINE7 - UDI-DI: 00708820657052 (unit), 10708820657059 (case), All Lots
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    January 5, 2026

  2. Reported by FDA DEVICE

    March 4, 2026

  3. RecallRadar source check

    March 11, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter

About This Product

Meijer STERILE saline wound wash is a first aid cleansing spray designed for wound irrigation and cleansing. Consumers typically buy it for minor cuts and abrasions to aid in the healing process.

Why This Is Dangerous

The product may lack the necessary sterility, increasing the risk of infection and complications when used on open wounds. Proper sterility is crucial for medical devices to ensure safety during treatment.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers may face health risks if they continue to use the affected saline wash. The recall requires immediate action to prevent potential infections.

Practical Guidance

How to identify if yours is affected

  1. Locate the model number MJSALINE7 on the product label.
  2. Check any packaging for additional identifiers related to the recall.
  3. Ensure the product is marked as sterile before use.

Where to find product info

The model number and production details can typically be found on the back of the can or on the product packaging.

What timeline to expect

Expect 4-6 weeks for refund processing once the product is returned to Medline Industries.

If the manufacturer is unresponsive

  • Document your correspondence with the company.
  • Follow up with a phone call if you do not receive a response within a week.
  • Consider filing a complaint with the FDA if the issue is not resolved.

How to prevent similar issues

  • Look for third-party certifications for sterility when purchasing similar products.
  • Avoid purchasing products with vague labeling regarding sterility.
  • Check for recalls regularly on the FDA website.

Documentation advice

Keep a copy of any receipts, correspondence with the manufacturer, and photos of the product for your records.

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Product Details

The recalled product is Meijer STERILE saline wound wash, First Aid Cleansing Spray, model number MJSALINE7. It comes in a 7.1 FL OZ (210 mL) spray can. The product was distributed worldwide, including the US, Bahamas, Bermuda, and Cayman Islands.

Key Facts

  • Recall date: January 5, 2026
  • Reported date: March 4, 2026
  • Quantity recalled: 104,608 units
  • Product sold worldwide
  • Stop using immediately, following manufacturer instructions

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Model Number MJSALINE7 - UDI-DI: 00708820657052 (unit)
10708820657059 (case)
All Lots
Affected States
ALL
Report Date
March 4, 2026
Recall Status
ACTIVE

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