Medline Industries Recalls Meijer Sterile Saline Wound Wash Over Sterility Concerns

FDA Recalls medium FDA · · United States

Medline Industries, LP is recalling 104,608 units of Meijer Sterile Saline Wound Wash because the product may not meet sterility assurance levels, posing a potential infection risk.

What Happened

Medline Industries, LP has initiated a voluntary recall of Meijer Sterile Saline Wound Wash. The recall was issued after it was identified that the manufacturer may not have met the minimum required sterility assurance levels for the product. Consequently, the product may not be fully sterile, which is a requirement for first aid cleansing sprays.

Which Products Are Affected

The recall involves 104,608 units of the following product:

  • Product Name: Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP SODIUM CHLORIDE
  • Size: 7.1 FL OZ (210 mL)
  • Model Number: MJSALINE7
  • UDI-DI: 00708820657052 (unit), 10708820657059 (case)
  • Lot Codes: All lots are affected.

Distribution was nationwide across the United States and included the Bahamas, Bermuda, and the Cayman Islands.

What You Should Do

Consumers should immediately stop using the affected Meijer Saline Wound Wash. Medline Industries, LP initiated the notification process via letter on January 5, 2026. Consumers seeking information regarding returns or specific instructions should contact Medline Industries, LP at their headquarters in Northfield, Illinois.

Why This Matters

Sterility is essential for products used to cleanse open wounds. If a product labeled as sterile does not meet sterility assurance levels, it may introduce contaminants to a wound, increasing the risk of infection and other health complications.

Source

Information provided by the FDA. Recall Number: Z-1435-2026.

Source: FDA Official Notice

Frequently Asked Questions

What is this fda recalls alert about?
Medline Industries, LP is recalling 104,608 units of Meijer Sterile Saline Wound Wash because the product may not meet sterility assurance levels, posing a potential infection risk.
Which agency issued this alert?
This alert was issued by FDA. The original notice is available at the source link at the bottom of this article.
How severe is this alert?
This alert is classified as "medium" severity. Stay informed and follow agency guidance.
What area is affected?
This alert affects United States. Check with FDA for the most current geographic scope.
Where can I find more fda recalls alerts?
Browse all fda recalls alerts on Areazine at areazine.com/recalls/fda/ for the latest updates from FDA and other agencies.