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

Products covered by this recall
#Product as published
1ANGIO PACK, Pack Number DYNJ50624A
2ANGIO PACK, Pack Number DYNJ30501F
3ANGIO PACK-LF, Pack Number DYNJ0954970G
4ANGIOGRAPHY 6 FRENCH PACK, Pack Number DYNJ33597J
5ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ38120B
6ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ42873
7ANGIOGRAPHY PACK, Pack Number DYNJ57498
8ANGIOGRAPHY PACK, Pack Number DYNJ52167A
9ANGIOGRAPHY PACK, Pack Number DYNJV0173I
10ANGIOGRAPHY TRAY-LF, Pack Number DYNJ58722A
11CATH LAB PACK, Pack Number DYNJ42912F
12CATH LAB PK, Pack Number DYNJ35643B
13CATH PACK-LF, Pack Number DYNJ0367643Q
14CRMS ANGIO PACK-LF, Pack Number PHS616026002A
15DEPAUL ANGIO CATH PACK, Pack Number DYNJ24542L
Lot codes and dates

15 of 15 products

Products covered by this recall
#BarcodesProduct as published
11088994280668340889942806684Lot Number 20BDB393A; 2) Pack Number DYNJ30501F: UDI/DI 10889942806683 (each) 40889942806684 (case)
21019348950563440193489505635Lot Number 21HBP134A; 3) Pack Number DYNJ0954970G: UDI/DI 10193489505634 (each) 40193489505635 (case)
31088994280201240889942802013Lot Number 21GMA850A; 4) Pack Number DYNJ33597J: UDI/DI 10889942802012 (each) 40889942802013 (case)
41088438972214540884389722146Lot Number 21IMD296A; 5) Pack Number DYNJ38120B: UDI/DI 10884389722145 (each) 40884389722146 (case)
51088827701129840888277011299Lot Number 21BBI114A; 6) Pack Number DYNJ42873: UDI/DI 10888277011298 (each) 40888277011299 (case)
61088994274574640889942745747Lot Number 23EBE560A; 7) Pack Number DYNJ57498: UDI/DI 10889942745746 (each) 40889942745747 (case)
71019348954110640193489541107Lot Number 21AMA569A; 8) Pack Number DYNJ52167A: UDI/DI 10193489541106 (each) 40193489541107 (case)
81088994296502140889942965022Lot Number 21GMB606A; 9) Pack Number DYNJV0173I: UDI/DI 10889942965021 (each) 40889942965022 (case)
91019348932969840193489329699Lot Number 23CLA070A; 10) Pack Number DYNJ58722A: UDI/DI 10193489329698 (each) 40193489329699 (case)
101019348978575340193489785754Lot Number 21IME955A; 11) Pack Number DYNJ42912F: UDI/DI 10193489785753 (each) 40193489785754 (case)
111019348922371240193489223713Lot Number 23LBU921Z; 12) Pack Number DYNJ35643B: UDI/DI 10193489223712 (each) 40193489223713 (case)
121019348964861440193489648615Lot Number 21BBG490A; 13) Pack Number DYNJ0367643Q: UDI/DI 10193489648614 (each) 40193489648615 (case)
131088994242937040889942429371Lot Number 23EBE428A; 14) Pack Number PHS616026002A: UDI/DI 10889942429370 (each) 40889942429371 (case)
141019348965111940193489651110Lot Number 23BBS889A; 15) Pack Number DYNJ24542L: UDI/DI 10193489651119 (each) 40193489651110 (case)
15Lot 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.

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:20 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.