Reported May 13, 2026 · Ongoing

Medline Convenience Kits

Medline Industries, LP

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 · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

Medline Convenience Kits

13 of 13 products

Products covered by this recall
Model / numberProduct as published
DYKMBNDL84AKIT SURG ONC EXCISION BREAST
DYKMBNDL87AKIT SURG ONC EXPLORATORY LAP
DYNDH1143CCT BIOPSY TRAY
DYNDH1873BIOPSY SPECIALS PACK
DYNDH1934BIOPSY SPECIALS PACK
DYNJ17489IBREAST BIOPSY PACK
DYNJ17558DC T BIOPSY TRAY-LF
DYNJ19063KRIGHT HEART BIOPSY TRAY
DYNJ48539VOR PACK-LF
DYNJ48539AVOR PACK-LF
DYNJ59897BIR BIOPSY PACK
DYNJ82998BREAST PACK
DYNJ910654LIVER BIOPSY KIT
Lot codes and dates

44 of 44 products

Products covered by this recall
#BarcodesProduct as published
11019532724048640195327240487Lot Number: 22IBQ267; 2) DYKMBNDL84A, UDI-DI: 10195327240486(each), 40195327240487(case)
21019532724048640195327240487Lot Number: 22IBU924; 3) DYKMBNDL84A, UDI-DI: 10195327240486(each), 40195327240487(case)
31019532724047940195327240470Lot Number: 23ABK216; 4) DYKMBNDL87A, UDI-DI: 10195327240479(each), 40195327240470(case)
41019532724047940195327240470Lot Number: 22LBK913; 5) DYKMBNDL87A, UDI-DI: 10195327240479(each), 40195327240470(case)
51019532724047940195327240470Lot Number: 22LBM302; 6) DYKMBNDL87A, UDI-DI: 10195327240479(each), 40195327240470(case)
61019532724047940195327240470Lot Number: 23ABU170; 7) DYKMBNDL87A, UDI-DI: 10195327240479(each), 40195327240470(case)
71019532724047940195327240470Lot Number: 23CBC364; 8) DYKMBNDL87A, UDI-DI: 10195327240479(each), 40195327240470(case)
81019348919333640193489193337Lot Number: 23CBL439; 9) DYNDH1143C, UDI-DI: 10193489193336(each), 40193489193337(case)
91019532748646440195327486465Lot Number: 22GBZ268; 10) DYNDH1873, UDI-DI: 10195327486464(each), 40195327486465(case)
101019532751972840195327519729Lot Number: 23KBK476; 11) DYNDH1934, UDI-DI: 10195327519728(each), 40195327519729(case)
111019532722478340195327224784Lot Number: 24FMF173; 12) DYNJ17489I, UDI-DI: 10195327224783(each), 40195327224784(case)
121019532750420540195327504206Lot Number: 23CBL337; 13) DYNJ17558D, UDI-DI: 10195327504205(each), 40195327504206(case)
131088827782802540888277828026Lot Number: 23JLB107; 14) DYNJ19063K, UDI-DI: 10888277828025(each), 40888277828026(case)
141088827790622840888277906229Lot Number: 24DBL079; 15) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case)
151088827790622840888277906229Lot Number: 20LME482; 16) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case)
161088827790622840888277906229Lot Number: 20LMF497; 17) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case)
171088827790622840888277906229Lot Number: 21JMC430; 18) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case)
181088827790622840888277906229Lot Number: 22BMH767; 19) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case)
191088827790622840888277906229Lot Number: 22EMD675; 20) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case)
201088827790622840888277906229Lot Number: 23AMC919; 21) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case)
Amount recalled
4064 units

This recall covers 42 products

The agency filed one notice per product. You are reading one of them; the other 41 are below.

29 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

This product could cause temporary or reversible health problems — stop using it.

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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, 6:55 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.