FDA recall, , Moderate risk
Medline Sterile Saline Wound Wash and Convenience Kits
Medline Sterile Saline Wound Wash may not meet sterility requirements.
Summary by Recall Canary from the FDA notice
What happened
Medline Industries, LP of Northfield, Illinois is recalling Medline Sterile Saline Wound Wash and Medline Convenience Kits because 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.
The recall began January 5, 2026, and was added to the FDA's Enforcement Report on February 20, 2026. The products were distributed worldwide, including the US Nationwide and the countries of Bahamas, Bermuda, and Cayman Islands.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
A UDI-DI is the device identifier printed with the barcode on the device label.
Medline Sterile Saline Wound Wash, Cleansing & Wound Irrigation, USP Normal Saline (0.9% Sodium Chloride), 7.1 fl oz (210 mL), DBD-Can,Spray,7.1-oz,Saline,Wound Wash,S, Model Number MDSALINE7
- UDI-DI
- 10193489089356
- 20193489089353
- Lot code
- All Lots
Nail Kit
- Model
- DYKM1528
Medline Convenience Kits
- UDI-DI
- 10889942689927
- 40889942689928
- Lot code
- 25BBO366
- 25ABI804
- 25ABF375
- 24JBL155
- 24IBG900
- 24FBT801
- 24FBC584
- 24DBB692
- 24BBL239
- 23KBO692
- 23IBT788
- 23HBJ026
- 23EBK780
- 23DBL149
- 23CBJ576
- DYKM1528
- 25IBP134
- UDI-DI
- 10193489586862
- 40193489586863
- 10193489796582
- 40193489796583
- 10195327419868
- 40195327419869
- 10195327610654
- 40195327610655
- 10888277572195
- 40888277572196
- Lot code
- 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
- 24CBG460
- 24ABO402
- 23LBU172
- 23KBK857
- 23KBJ794
- 23JBM608
- 23IBQ747
- 23IBO843
- 23IBO844
- 23HBT781
- 23FBK991
- 23FBC676
- 23EBG472
- 23CBW700
- 23CBM546
- DYKTRUNK1
- 25IBL812
- 25IBH378
- UDI-DI
- 10889942819362
- 40889942819363
- Lot code
- 25CBS147
- 25CBJ329
- 25ABU209
- 24DBJ364
- 24DBB718
- 23JBV524
- 23IBU998
- 23IBF119
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
- UDI-DI
- 00708820657052
- 10708820657059
- Lot code
- All Lots
Recall details
- Company began the recall
- Sold in
Worldwide distribution - US Nationwide and the countries of Bahamas, Bermuda, Cayman Islands.
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Sterility problem
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98319
- Recall numbers
- Z-1431-2026 to Z-1435-2026
All recalls from Medline Industries, LP
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
