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
7 of 7 products
| # | Product as published |
|---|---|
| 1 | ARTHROSCOPY PACK, Pack Number DYNJHS0101I |
| 2 | ARTHROSCOPY PACK-LF, Pack Number DYNJ0390808F |
| 3 | ARTHROSCOPY PACK-LF, Pack Number DYNJ23150J |
| 4 | ARTHROSCOPY PACK-LF, Pack Number DYNJ21233O |
| 5 | ARTHROSCOPY PACK-LF, Pack Number DYNJ21233O |
| 6 | ARTHROSCOPY TRAY, Pack Number DYNJ46435A |
| 7 | KNEE ARTHROSCOPY PACK, Pack Number DYNJ50120D |
- Lot codes and dates
7 of 7 products
Products covered by this recall # Barcodes Product as published 1 1088994224459140889942244592Lot Number 21LBA780A; 2) Pack Number DYNJ0390808F: UDI/DI 10889942244591 (each) 40889942244592 (case) 2 1088827774223940888277742230Lot Number 21JMG164A; 3) Pack Number DYNJ23150J: UDI/DI 10888277742239 (each) 40888277742230 (case) 3 1088994254387840889942543879Lot Number 21LMF991A; 4) Pack Number DYNJ21233O: UDI/DI 10889942543878 (each) 40889942543879 (case) 4 1088994254387840889942543879Lot Number 22GBQ106M; 5) Pack Number DYNJ21233O: UDI/DI 10889942543878 (each) 40889942543879 (case) 5 1088994267090140889942670902Lot Number 22JBA123Z; 6) Pack Number DYNJ46435A: UDI/DI 10889942670901 (each) 40889942670902 (case) 6 1019532719565640195327195657Lot Number 23LMG014A; 7) Pack Number DYNJ50120D: UDI/DI 10195327195656 (each) 40195327195657 (case) 7 Lot Number 22JBG571Z - Amount recalled
- 186 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.
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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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