Reported Oct 30, 2024 · Ongoing

Medline brand medical procedure convenience 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?

110 of 110 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ19492L4019532736858710195327368586UDI/DI 40195327368587 (each), 10195327368586 (case), Lot Numbers: 24ABE741
DYNJ22354L4019532723992410195327239923UDI/DI 40195327239924 (each), 10195327239923 (case), Lot Numbers: 23LBN139
DYNJ24573K4019532714430310195327144302UDI/DI 40195327144303 (each), 10195327144302 (case), Lot Numbers: 23KBB931
DYNJ30327A4019348999708910193489997088UDI/DI 40193489997089 (each), 10193489997088 (case), Lot Numbers: 24ABB714
DYNJ36868F4088827789706010888277897069UDI/DI 40888277897060 (each), 10888277897069 (case), Lot Numbers: 23KBD160
DYNJ40811A4088827701463410888277014633UDI/DI 40888277014634 (each), 10888277014633 (case), Lot Numbers: 23KBE584
DYNJ41769A4088827726782510888277267824UDI/DI 40888277267825 (each), 10888277267824 (case), Lot Numbers: 23KBB744
DYNJ418614088827702074110888277020740UDI/DI 40888277020741 (each), 10888277020740 (case), Lot Numbers: 23KBB746
DYNJ439114088827707361710888277073616UDI/DI 40888277073617 (each), 10888277073616 (case), Lot Numbers: 23LBQ741
DYNJ44748I4019348927345910193489273458UDI/DI 40193489273459 (each), 10193489273458 (case), Lot Numbers: 23LBP074
DYNJ45344G4019532740292210195327402921UDI/DI 40195327402922 (each), 10195327402921 (case), Lot Numbers: 23LBU068
DYNJ47275A4088827757194610888277571945UDI/DI 40888277571946 (each), 10888277571945 (case), Lot Numbers: 24ABE470
DYNJ49412B4088994293527810889942935277UDI/DI 40889942935278 (each), 10889942935277 (case), Lot Numbers: 24ABD256
DYNJ50948A4019532711755010195327117559UDI/DI 40195327117550 (each), 10195327117559 (case), Lot Numbers: 24ABC786
DYNJ50948A4019532711755010195327117559UDI/DI 40195327117550 (each), 10195327117559 (case), Lot Numbers: 23KBA350
DYNJ51590A4019348972138710193489721386UDI/DI 40193489721387 (each), 10193489721386 (case), Lot Numbers: 23LBN087
DYNJ51590A4019348972138710193489721386UDI/DI 40193489721387 (each), 10193489721386 (case), Lot Numbers: 23KBE531
DYNJ51821B4019348996337410193489963373UDI/DI 40193489963374 (each), 10193489963373 (case), Lot Numbers: 23KBE568
DYNJ53097C4088994272137610889942721375UDI/DI 40889942721376 (each), 10889942721375 (case), Lot Numbers: 24ABC180
DYNJ539444088994245068910889942450688UDI/DI 40889942450689 (each), 10889942450688 (case), Lot Numbers: 23LBR325
Amount recalled
27,906 units

This recall covers 34 products

The agency filed one notice per product. You are reading one of them; the other 33 are below.

21 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.

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.