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 | AV FISTULA PACK-LF, Pack Number DYNJ0826753O |
| 2 | BARRINGTON ACCESSORY TTL KNEE, Pack Number DYNJ56717A |
| 3 | CVL INSERTION PACK, Pack Number CVI5065 |
| 4 | KT DR VELASCO FISTULA PACK, Pack Number DYNJ46648D |
| 5 | PICC ABSCESS PACK-LF, Pack Number DYNJ0774005G |
| 6 | PICC/RAD SPEC PROC 0906165-LF, Pack Number DYNJ32773G |
| 7 | VAP PACK-LF, Pack Number PHS656578F |
- Lot codes and dates
7 of 7 products
Products covered by this recall # Barcodes Product as published 1 1088994289794040889942897941Lot Number 23GMB253A; 2) Pack Number DYNJ56717A : UDI/DI 10889942897940 (each) 40889942897941 (case) 2 1019532750436640195327504367Lot Number 21EBM603A; 3) Pack Number CVI5065 : UDI/DI 10195327504366 (each) 40195327504367 (case) 3 1019348975524440193489755245Lot Number 23LMH242A; 4) Pack Number DYNJ46648D : UDI/DI 10193489755244 (each) 40193489755245 (case) 4 1019348927148540193489271486Lot Number 20HMC528A; 5) Pack Number DYNJ0774005G : UDI/DI 10193489271485 (each) 40193489271486 (case) 5 1019348976613440193489766135Lot Number 21EMA842Z; 6) Pack Number DYNJ32773G : UDI/DI 10193489766134 (each) 40193489766135 (case) 6 1088994280453540889942804536Lot Number 21IMG907A; 7) Pack Number PHS656578F : UDI/DI 10889942804535 (each) 40889942804536 (case) 7 Lot Number 20LKB006A - Amount recalled
- 398
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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