FDA-Device2026-03-04Class IIPROCESSING DEFECT
Meijer sterile saline wound wash recalled for potential sterility failure
What this means
Meijer sterile saline wound wash (0.9% sodium chloride, 7.1 fl oz) may not have been manufactured to meet required sterility standards. The manufacturer did not follow proper sterilization procedures for this wound-cleaning product. All lots of model MJSALINE7 are affected.
- Stop using the product immediately if you have it
- Do not use on wounds or for first aid
- Dispose of the saline spray safely
- Contact Medline Industries or check Meijer's website for a refund or replacement
The agency's original wording
Hazard
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.
Intended for
All ages
Illnesses reported
None reported
Sold states
Worldwide distribution - US Nationwide and the countries of Bahamas, Bermuda, Cayman Islands.
Affected count
104,608 units
Manufactured in
3 Lakes Dr, N/A, Northfield, IL, United States
Products
Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP SODIUM CHLORIDE, 7.1FL OZ (210 mL), DBD-CAN,SPRAY,7.1-OZ,SALINE,WOUND WASH,S, Model Number MJSALINE7
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1435-2026More Medline recalls
- FDA-Device2026-09-09Medline Convenience Kits recalled for potential sterility breach in antiseptic applicators
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for contamination risk
- FDA-Device2026-09-09Medline Convenience Kits recalled for sterility packaging breach risk
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for defective packaging seals
- FDA-Device2026-09-09Medline Arterial Line Insertion Kit recalled for sterility packaging breach risk
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