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

17 of 17 products

Products covered by this recall
#Product as published
1BREAST PACK-LF, Pack Number DYNJ0956628O
2BREAST SURGERY FOAKS, Pack Number DYNJ63577C
3CHEST BREAST -LF, Pack Number DYNJCEN04C
4DIEP PACK, Pack Number DYNJ60669G
5FACE LIFT PACK, Pack Number DYNJ64670B
6FREE FLAP A PACK, Pack Number DYNJ40647G
7IPMC BREAST PACK-LF, Pack Number DYNJ0665560D
8OCULAR PLASTICS PACK, Pack Number DYNJ40356A
9OCULOPLASTY PACK-LF, Pack Number DYNJ0252232U
10PACK MASTECTOMY COMBO CHRG, Pack Number DYNJ60232A
11PLASTIC GENERAL SURGERY - OSC, Pack Number DYNJ43576A
12PLASTIC PACK, Pack Number DYNJ00264L
13PLASTIC PACK, Pack Number DYNJ49742B
14PLASTIC PK II, Pack Number DYNJ14039B
15PLASTIC-GENERAL SURGERY PACK, Pack Number DYNJ09866U
16PLASTICS FACIAL PACK ST MARY, Pack Number DYNJ45861B
17PLASTICS PACK, Pack Number DYNJ68288A
Lot codes and dates

17 of 17 products

Products covered by this recall
#BarcodesProduct as published
11019348926714340193489267144Lot Number 21BBH575A; 2) Pack Number DYNJ63577C: UDI/DI 10193489267143 (each) 40193489267144 (case)
21019348980541340193489805414Lot Number 21BBI089A; 3) Pack Number DYNJCEN04C: UDI/DI 10193489805413 (each) 40193489805414 (case)
31088994279494240889942794943Lot Number 21BBI544A; 4) Pack Number DYNJ60669G: UDI/DI 10889942794942 (each) 40889942794943 (case)
41088994257570140889942575702Lot Number 21EME131A; 5) Pack Number DYNJ64670B: UDI/DI 10889942575701 (each) 40889942575702 (case)
51019348927097640193489270977Lot Number 21IME484A; 6) Pack Number DYNJ40647G: UDI/DI 10193489270976 (each) 40193489270977 (case)
61019532708979540195327089796Lot Number 21IMH836A; 7) Pack Number DYNJ0665560D: UDI/DI 10195327089795 (each) 40195327089796 (case)
71019348922833540193489228336Lot Number 22CMB464A; 8) Pack Number DYNJ40356A: UDI/DI 10193489228335 (each) 40193489228336 (case)
81019532721733440195327217335Lot Number 22JBF484Z; 9) Pack Number DYNJ0252232U: UDI/DI 10195327217334 (each) 40195327217335 (case)
91019532722245140195327222452Lot Number 22JBG465Z; 10) Pack Number DYNJ60232A: UDI/DI 10195327222451 (each) 40195327222452 (case)
101019348992011640193489920117Lot Number 22JBN921Z; 11) Pack Number DYNJ43576A: UDI/DI 10193489920116 (each) 40193489920117 (case)
111019348980186640193489801867Lot Number 22JBU153Z; 12) Pack Number DYNJ00264L: UDI/DI 10193489801866 (each) 40193489801867 (case)
121019532721026740195327210268Lot Number 22JBU265A; 13) Pack Number DYNJ49742B: UDI/DI 10195327210267 (each) 40195327210268 (case)
131019348932449540193489324496Lot Number 22JBV346A; 14) Pack Number DYNJ14039B: UDI/DI 10193489324495 (each) 40193489324496 (case)
141019532723008140195327230082Lot Number 22JBW642A; 15) Pack Number DYNJ09866U: UDI/DI 10195327230081 (each) 40195327230082 (case)
151019348927651040193489276511Lot Number 22JBY434A; 16) Pack Number DYNJ45861B: UDI/DI 10193489276510 (each) 40193489276511 (case)
161019348927651040193489276511Lot Number 22KBC920Z; 17) Pack Number DYNJ68288A: UDI/DI 10193489276510 (each) 40193489276511 (case)
17Lot Number 22KBC927Z
Amount recalled
1228 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, 7:44 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.