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
15 of 15 products
| # | Product as published |
|---|---|
| 1 | ANGIO PACK, Pack Number DYNJ50624A |
| 2 | ANGIO PACK, Pack Number DYNJ30501F |
| 3 | ANGIO PACK-LF, Pack Number DYNJ0954970G |
| 4 | ANGIOGRAPHY 6 FRENCH PACK, Pack Number DYNJ33597J |
| 5 | ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ38120B |
| 6 | ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ42873 |
| 7 | ANGIOGRAPHY PACK, Pack Number DYNJ57498 |
| 8 | ANGIOGRAPHY PACK, Pack Number DYNJ52167A |
| 9 | ANGIOGRAPHY PACK, Pack Number DYNJV0173I |
| 10 | ANGIOGRAPHY TRAY-LF, Pack Number DYNJ58722A |
| 11 | CATH LAB PACK, Pack Number DYNJ42912F |
| 12 | CATH LAB PK, Pack Number DYNJ35643B |
| 13 | CATH PACK-LF, Pack Number DYNJ0367643Q |
| 14 | CRMS ANGIO PACK-LF, Pack Number PHS616026002A |
| 15 | DEPAUL ANGIO CATH PACK, Pack Number DYNJ24542L |
- Lot codes and dates
15 of 15 products
Products covered by this recall # Barcodes Product as published 1 1088994280668340889942806684Lot Number 20BDB393A; 2) Pack Number DYNJ30501F: UDI/DI 10889942806683 (each) 40889942806684 (case) 2 1019348950563440193489505635Lot Number 21HBP134A; 3) Pack Number DYNJ0954970G: UDI/DI 10193489505634 (each) 40193489505635 (case) 3 1088994280201240889942802013Lot Number 21GMA850A; 4) Pack Number DYNJ33597J: UDI/DI 10889942802012 (each) 40889942802013 (case) 4 1088438972214540884389722146Lot Number 21IMD296A; 5) Pack Number DYNJ38120B: UDI/DI 10884389722145 (each) 40884389722146 (case) 5 1088827701129840888277011299Lot Number 21BBI114A; 6) Pack Number DYNJ42873: UDI/DI 10888277011298 (each) 40888277011299 (case) 6 1088994274574640889942745747Lot Number 23EBE560A; 7) Pack Number DYNJ57498: UDI/DI 10889942745746 (each) 40889942745747 (case) 7 1019348954110640193489541107Lot Number 21AMA569A; 8) Pack Number DYNJ52167A: UDI/DI 10193489541106 (each) 40193489541107 (case) 8 1088994296502140889942965022Lot Number 21GMB606A; 9) Pack Number DYNJV0173I: UDI/DI 10889942965021 (each) 40889942965022 (case) 9 1019348932969840193489329699Lot Number 23CLA070A; 10) Pack Number DYNJ58722A: UDI/DI 10193489329698 (each) 40193489329699 (case) 10 1019348978575340193489785754Lot Number 21IME955A; 11) Pack Number DYNJ42912F: UDI/DI 10193489785753 (each) 40193489785754 (case) 11 1019348922371240193489223713Lot Number 23LBU921Z; 12) Pack Number DYNJ35643B: UDI/DI 10193489223712 (each) 40193489223713 (case) 12 1019348964861440193489648615Lot Number 21BBG490A; 13) Pack Number DYNJ0367643Q: UDI/DI 10193489648614 (each) 40193489648615 (case) 13 1088994242937040889942429371Lot Number 23EBE428A; 14) Pack Number PHS616026002A: UDI/DI 10889942429370 (each) 40889942429371 (case) 14 1019348965111940193489651110Lot Number 23BBS889A; 15) Pack Number DYNJ24542L: UDI/DI 10193489651119 (each) 40193489651110 (case) 15 Lot Number 20FBN798A - Amount recalled
- 1939 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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