Reported Apr 2, 2025 · Ongoing
Medline procedure kits labeled as
MEDLINE INDUSTRIES, LP - Northfield
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline procedure kits labeled as
10 of 10 products
| # | Product as published |
|---|---|
| 1 | C SECTION, Pack Number DYNJ57622 |
| 2 | C SECTION PACK, Pack Number DYNJ48483B |
| 3 | C SECTION PACK, Pack Number DYNJ61573 |
| 4 | C SECTION PACK, Pack Number DYNJ66801 |
| 5 | C SECTION PACK-LF, Pack Number DYNJ0367951P |
| 6 | C SECTION PACK-LF, Pack Number DYNJ55345D |
| 7 | C-SECTION PACK, Pack Number DYNJ04521J |
| 8 | C-SECTION PACK, Pack Number DYNJ32632F |
| 9 | C-SECTION PACK, Pack Number DYNJ65961B |
| 10 | SMJ C-SECTION PACK-LF, Pack Number DYNJ38582J |
- Lot codes and dates
10 of 10 products
Products covered by this recall # Barcodes Product as published 1 1019348965940540193489659406Lot Number 20LMF902A; 2) Pack Number DYNJ48483B: UDI/DI 10193489659405 (each) 40193489659406 (case) 2 1019348960107740193489601078Lot Number 20CKB746A; 3) Pack Number DYNJ61573: UDI/DI 10193489601077 (each) 40193489601078 (case) 3 1019348938400040193489384001Lot Number 22CMB584A; 4) Pack Number DYNJ66801: UDI/DI 10193489384000 (each) 40193489384001 (case) 4 1019348996692340193489966924Lot Number 22GBW063A; 5) Pack Number DYNJ0367951P: UDI/DI 10193489966923 (each) 40193489966924 (case) 5 1019532717372240195327173723Lot Number 21IMH644A; 6) Pack Number DYNJ55345D: UDI/DI 10195327173722 (each) 40195327173723 (case) 6 1019348955583740193489555838Lot Number 22GBJ830A; 7) Pack Number DYNJ04521J: UDI/DI 10193489555837 (each) 40193489555838 (case) 7 1019348988896640193489888967Lot Number 21HMA851A; 8) Pack Number DYNJ32632F: UDI/DI 10193489888966 (each) 40193489888967 (case) 8 1019348998430940193489984300Lot Number 21IMD959A; 9) Pack Number DYNJ65961B: UDI/DI 10193489984309 (each) 40193489984300 (case) 9 1019348952824440193489528245Lot Number 23LMG679A; 10) Pack Number DYNJ38582J: UDI/DI 10193489528244 (each) 40193489528245 (case) 10 Lot Number 21IMF094A - Amount recalled
- 605 units
This recall covers 29 products
The agency filed one notice per product. You are reading one of them; the other 28 are below.
16 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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