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
| Model / number | Product as published |
|---|---|
DYKMBNDL84A | KIT SURG ONC EXCISION BREAST |
DYKMBNDL87A | KIT SURG ONC EXPLORATORY LAP |
DYNDH1143C | CT BIOPSY TRAY |
DYNDH1873 | BIOPSY SPECIALS PACK |
DYNDH1934 | BIOPSY SPECIALS PACK |
DYNJ17489I | BREAST BIOPSY PACK |
DYNJ17558D | C T BIOPSY TRAY-LF |
DYNJ19063K | RIGHT HEART BIOPSY TRAY |
DYNJ48539 | VOR PACK-LF |
DYNJ48539A | VOR PACK-LF |
DYNJ59897B | IR BIOPSY PACK |
DYNJ82998 | BREAST PACK |
DYNJ910654 | LIVER BIOPSY KIT |
- Lot codes and dates
44 of 44 products
Products covered by this recall # Barcodes Product as published 1 1019532724048640195327240487Lot Number: 22IBQ267; 2) DYKMBNDL84A, UDI-DI: 10195327240486(each), 40195327240487(case) 2 1019532724048640195327240487Lot Number: 22IBU924; 3) DYKMBNDL84A, UDI-DI: 10195327240486(each), 40195327240487(case) 3 1019532724047940195327240470Lot Number: 23ABK216; 4) DYKMBNDL87A, UDI-DI: 10195327240479(each), 40195327240470(case) 4 1019532724047940195327240470Lot Number: 22LBK913; 5) DYKMBNDL87A, UDI-DI: 10195327240479(each), 40195327240470(case) 5 1019532724047940195327240470Lot Number: 22LBM302; 6) DYKMBNDL87A, UDI-DI: 10195327240479(each), 40195327240470(case) 6 1019532724047940195327240470Lot Number: 23ABU170; 7) DYKMBNDL87A, UDI-DI: 10195327240479(each), 40195327240470(case) 7 1019532724047940195327240470Lot Number: 23CBC364; 8) DYKMBNDL87A, UDI-DI: 10195327240479(each), 40195327240470(case) 8 1019348919333640193489193337Lot Number: 23CBL439; 9) DYNDH1143C, UDI-DI: 10193489193336(each), 40193489193337(case) 9 1019532748646440195327486465Lot Number: 22GBZ268; 10) DYNDH1873, UDI-DI: 10195327486464(each), 40195327486465(case) 10 1019532751972840195327519729Lot Number: 23KBK476; 11) DYNDH1934, UDI-DI: 10195327519728(each), 40195327519729(case) 11 1019532722478340195327224784Lot Number: 24FMF173; 12) DYNJ17489I, UDI-DI: 10195327224783(each), 40195327224784(case) 12 1019532750420540195327504206Lot Number: 23CBL337; 13) DYNJ17558D, UDI-DI: 10195327504205(each), 40195327504206(case) 13 1088827782802540888277828026Lot Number: 23JLB107; 14) DYNJ19063K, UDI-DI: 10888277828025(each), 40888277828026(case) 14 1088827790622840888277906229Lot Number: 24DBL079; 15) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case) 15 1088827790622840888277906229Lot Number: 20LME482; 16) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case) 16 1088827790622840888277906229Lot Number: 20LMF497; 17) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case) 17 1088827790622840888277906229Lot Number: 21JMC430; 18) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case) 18 1088827790622840888277906229Lot Number: 22BMH767; 19) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case) 19 1088827790622840888277906229Lot Number: 22EMD675; 20) DYNJ48539, UDI-DI: 10888277906228(each), 40888277906229(case) 20 1088827790622840888277906229Lot 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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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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