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
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 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.
Recall announced
January 5, 2026
Reported by FDA DEVICE
March 4, 2026
RecallRadar source check
March 11, 2026
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
- Locate the model number MJSALINE7 on the product label.
- Check any packaging for additional identifiers related to the recall.
- 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
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Safety Guide
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