Home/Recalls/FDA-Z-1435-2026
FDA DevicesClass II

Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP SODIUM CHL...

Published: March 4, 2026Recall ID: Z-1435-2026Category: devicesCountry: US

Reason for Recall / 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.

Product Description & Identification

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

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98319
Address 13 Lakes Dr
Address 2N/A
Code infoModel Number MJSALINE7 - UDI-DI: 00708820657052 (unit), 10708820657059 (case), All Lots
Postal code60093-2753
Report date20260304
Product typeDevices
Product quantity104,608 units
Reason for recallMedline 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.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260105
Initial firm notificationLetter
Center classification date20260220

Overview

  • Recalling FirmMedline Industries, LP
  • StatusOngoing
  • Risk LevelClass II
  • DistributionWorldwide distribution - US Nationwide and the countries of Bahamas, Bermuda, Cayman Islands.
Official Agency Alert