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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Home Healthcare

Medline and Meijer Sterile Saline Wound Wash Recalled for Sterility Concerns

Agency Publication Date: February 20, 2026
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Summary

Medline Industries, LP is recalling approximately 3.7 million units of Sterile Saline Wound Wash and various medical convenience kits. The manufacturer identified that these products may not meet the minimum required sterility assurance levels, meaning they may not be completely sterile. Affected brands include Medline and Meijer, as well as several specialized medical kits containing the saline wash. Consumers and healthcare providers should immediately stop using the affected products to avoid potential infection.

Risk

Using a wound wash that is not properly sterile can introduce bacteria or other contaminants directly into open wounds, significantly increasing the risk of serious infection. No injuries have been reported to date, but the lack of sterility assurance poses a medium risk to patient safety.

What You Should Do

  1. Identify if you have the recalled product by checking the brand name (Medline or Meijer) and the model numbers MDSALINE7, MJSALINE7, POD14214, DYKM1361A, DYKM2013, DYKM2013A, DYKM2699, DYKTRUNK1, or DYKM1528.
  2. Check the lot number and UDI-DI on your product packaging or convenience kit label. See the Affected Products section below for the full list of affected codes.
  3. Stop using the product immediately. Return it to the place of purchase for a refund or replacement, throw it away, or contact your healthcare provider or Medline Industries, LP for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Stop using and throw the product away.

Affected Products

Product: Medline Sterile Saline Wound Wash, Cleansing & Wound Irrigation, USP Normal Saline (0.9% Sodium Chloride) (7.1 FL OZ)
Model / REF:
MDSALINE7
UDI:
10193489089356
20193489089353

All Lots affected.

Product: Medline Convenience Kits: Nail Kit
Model / REF:
POD14214
Lot Numbers:
25CBS147
25CBJ329
25ABU209
24DBJ364
24DBB718
23JBV524
23IBU998
23IBF119
UDI:
10889942819362
40889942819363
Product: Medline Convenience Kits: Trunk Kits (Various Models)
Variants: TRUNK KIT W/EXPIRATION, TRUNK KIT 1EA, RN TRUNK KIT, TRUNK KIT
Model / REF:
DYKM1361A
DYKM2013
DYKM2013A
DYKM2699
DYKTRUNK1
Lot Numbers (67):
25JBG340
25EBV829
25CBM029
25BBI797
25ABW687
23EBN045
23DBM064
25HBB845
25GBS259
25DBR145
25BBS769
24KBJ466
24JBQ815
24IBU526
23IBJ540
23HBP844
23HBE308
23GBT102
25DLA344
25CLA657
24GLB208
24ELA332
25HBS451
25HBS450
25HBE908
25HBE909
25GBM037
25GBK565
25FBL177
25EBP727
25EBO749
25DBQ021
25DBD942
25DBA345
25BBU730
25BBS503
25ABM247
24KBN725
24KBE264
24IBH956
24IBH955
24IBH957
24HBQ854
24HBO200
24GBN624
24FBH929
24FBG790
24FBD096
24DBS507
24DBC075
UDI:
10193489586862
40193489586863
10193489796582
40193489796583
10195327419868
40195327419869
10195327610654
40195327610655
10888277572195
40888277572196
Product: Medline Convenience Kits: Nail Kit (DYKM1528)
Model / REF:
DYKM1528
Lot Numbers:
25BBO366
25ABI804
25ABF375
24JBL155
24IBG900
24FBT801
24FBC584
24DBB692
24BBL239
23KBO692
23IBT788
23HBJ026
23EBK780
23DBL149
23CBJ576
25IBP134
UDI:
10889942689927
40889942689928
Product: Meijer STERILE saline wound wash, First Aid Cleansing Spray (7.1 FL OZ)
Model / REF:
MJSALINE7
UDI:
00708820657052
10708820657059

All Lots affected.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98319
Status: Active
Manufacturer: Medline Industries, LP
Sold By: Meijer; Medline Industries; Healthcare facilities; Specialty retailers
Manufactured In: United States
Units Affected: 5 products (3,578,805 units; 1640 units; 10550 units (495 additional units 3/27/26); 8773 units (594 additional units 3/27/26); 104,608 units)
Distributed To: Nationwide
Agency Last Updated: April 7, 2026

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.