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

31 of 31 products

Products covered by this recall
#Product as published
1AOP/BASIC EYE PACK-LF, Pack Number DYNJ0589795V
2CATARACT CM-LF, Pack Number DYNJ39921B
3CATARACT EYE, Pack Number DYNJ45662C
4CATARACT PACK, Pack Number DYNJ56056B
5CATARACT PACK, Pack Number DYNJ56553B
6CATARACT PACK, Pack Number DYNJ0417156G
7CATARACT PACK, Pack Number DYNJ60411A
8CATARACT PACK, Pack Number DYNJ52649F
9CATARACT PACK - 30843, Pack Number DYNJVB1076B
10CATARACT PACK-LF, Pack Number DYNJ0317858M
11CATARACT-LF, Pack Number DYNJ40081F
12ENT PACK, Pack Number DYNJ38916B
13EYE CATARACT PK, Pack Number DYNJ46557K
14EYE CATARACT PK, Pack Number DYNJ46557L
15EYE PACK, Pack Number DYNJ48800C
16EYE PACK, Pack Number DYNJ38494G
17EYE PACK, Pack Number DYNJ21134A
18EYE PACK 1, Pack Number DYNJHTEY01
19EYE PACK II-LF, Pack Number DYNJ50237A
20EYE PBM-LF, Pack Number DYNJ0190619G
Lot codes and dates

31 of 31 products

Products covered by this recall
#BarcodesProduct as published
11019532717636540195327176366Lot Number 23LMF853A; 2) Pack Number DYNJ39921B: UDI/DI 10195327176365 (each) 40195327176366 (case)
21019348955663640193489556637Lot Number 24AMI654A; 3) Pack Number DYNJ45662C: UDI/DI 10193489556636 (each) 40193489556637 (case)
31019348963534840193489635349Lot Number 20EBE340A; 4) Pack Number DYNJ56056B: UDI/DI 10193489635348 (each) 40193489635349 (case)
41019348976196240193489761963Lot Number 20JKA823A; 5) Pack Number DYNJ56553B: UDI/DI 10193489761962 (each) 40193489761963 (case)
51088994206742840889942067429Lot Number 21IMG706A; 6) Pack Number DYNJ0417156G: UDI/DI 10889942067428 (each) 40889942067429 (case)
61019532722139340195327221394Lot Number 22IMG784A; 7) Pack Number DYNJ60411A: UDI/DI 10195327221393 (each) 40195327221394 (case)
71019532735731340195327357314Lot Number 22IMG811A; 8) Pack Number DYNJ52649F: UDI/DI 10195327357313 (each) 40195327357314 (case)
81019532706273640195327062737Lot Number 23HME435A; 9) Pack Number DYNJVB1076B: UDI/DI 10195327062736 (each) 40195327062737 (case)
91088994239978940889942399780Lot Number 23CLA046A; 10) Pack Number DYNJ0317858M: UDI/DI 10889942399789 (each) 40889942399780 (case)
101019532706837040195327068371Lot Number 22IMD667A; 11) Pack Number DYNJ40081F: UDI/DI 10195327068370 (each) 40195327068371 (case)
111019348996986340193489969864Lot Number 23IMC700A; 12) Pack Number DYNJ38916B: UDI/DI 10193489969863 (each) 40193489969864 (case)
121019348998722540193489987226Lot Number 23HMC484A; 13) Pack Number DYNJ46557K: UDI/DI 10193489987225 (each) 40193489987226 (case)
131019532746687940195327466870Lot Number 23FMF487A; 14) Pack Number DYNJ46557L: UDI/DI 10195327466879 (each) 40195327466870 (case)
141019348960217340193489602174Lot Number 23LMF146A; 15) Pack Number DYNJ48800C: UDI/DI 10193489602173 (each) 40193489602174 (case)
151019348940489040193489404891Lot Number 22IME600A; 16) Pack Number DYNJ38494G: UDI/DI 10193489404890 (each) 40193489404891 (case)
161008019681832740080196818328Lot Number 22IMF477A; 17) Pack Number DYNJ21134A: UDI/DI 10080196818327 (each) 40080196818328 (case)
171088827707875840888277078759Lot Number 23GMC030A; 18) Pack Number DYNJHTEY01: UDI/DI 10888277078758 (each) 40888277078759 (case)
181019532701396740195327013968Lot Number 23HBT532A; 19) Pack Number DYNJ50237A: UDI/DI 10195327013967 (each) 40195327013968 (case)
191019348944258840193489442589Lot Number 21KBW890A; 20) Pack Number DYNJ0190619G: UDI/DI 10193489442588 (each) 40193489442589 (case)
201019532700160540195327001606Lot Number 21IMH127A; 21) Pack Number DYNJ66623A: UDI/DI 10195327001605 (each) 40195327001606 (case)
Amount recalled
5,132 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, 7:47 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.