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
57 of 57 products
| Model / number | Product as published |
|---|---|
00-401824AB | ANGIO PROCEDURE PACK |
CDS985094F | OR ARTERIOGRAM |
DYK1060193I | INTRAVASOR CATH KIT |
DYKMBNDL153 | KIT SURG ONC LAP DIAG/CV CATH |
DYKMBNDL4A | KIT ACES INSERT PERCUTANEOUS T |
DYKMBNDL4B | KIT ACES INSERT PERCUTANEOUS T |
DYNDA2076C | VEIN PROCEDURE KIT |
DYNJ0150605AC | CARDIAC CATH PACK-LF |
DYNJ0368386D | CARDIAC CATH PACK-LF |
DYNJ0648473Y | CATH LAB PACK-LF |
DYNJ0803367I | NBMC CATH PACK-LF |
DYNJ0928124C | RADIOLOGY PACK-LF |
DYNJ0954970I | ANGIO PACK-LF |
DYNJ16803D | SPECIALS TRAY RADIOLOGY |
DYNJ19946M | CARDIAC CATH PACK |
DYNJ30955I | CATH LAB PACK |
DYNJ31773K | CATH LAB PACK |
DYNJ33061D | CATH PACK-LF |
DYNJ33620D | DB CCL OAKWOOD PACK-LF |
DYNJ35300M | CARDIAC CATH PACK MRH-LF |
- Lot codes and dates
278 of 278 products
Products covered by this recall # Barcodes Product as published 1 1019845908916940198459089160Lot Number: 24IBQ637; 2) 00-401824AB, UDI-DI: 10198459089169(each), 40198459089160(case) 2 1019845908916940198459089160Lot Number: 24KBF279; 3) 00-401824AB, UDI-DI: 10198459089169(each), 40198459089160(case) 3 1019845908916940198459089160Lot Number: 24LBF132; 4) 00-401824AB, UDI-DI: 10198459089169(each), 40198459089160(case) 4 1019845908916940198459089160Lot Number: 25CBJ807; 5) 00-401824AB, UDI-DI: 10198459089169(each), 40198459089160(case) 5 1019845908916940198459089160Lot Number: 25DBO471; 6) 00-401824AB, UDI-DI: 10198459089169(each), 40198459089160(case) 6 1019532765764240195327657643Lot Number: 25GBK506; 7) CDS985094F, UDI-DI: 10195327657642(each), 40195327657643(case) 7 1088438987173740884389871738Lot Number: 25AMG933; 8) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 8 1088438987173740884389871738Lot Number: 22KBQ113; 9) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 9 1088438987173740884389871738Lot Number: 23ABU376; 10) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 10 1088438987173740884389871738Lot Number: 23DBD193; 11) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 11 1088438987173740884389871738Lot Number: 23GBT819; 12) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 12 1088438987173740884389871738Lot Number: 23HBQ238; 13) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 13 1088438987173740884389871738Lot Number: 23IBR569; 14) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 14 1088438987173740884389871738Lot Number: 23KBH770; 15) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 15 1088438987173740884389871738Lot Number: 23LBO849; 16) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 16 1088438987173740884389871738Lot Number: 24ABW181; 17) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 17 1088438987173740884389871738Lot Number: 24EBM208; 18) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 18 1088438987173740884389871738Lot Number: 24GBA239; 19) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 19 1088438987173740884389871738Lot Number: 24IBE619; 20) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) 20 1088438987173740884389871738Lot Number: 24JBA719; 21) DYK1060193I, UDI-DI: 10884389871737(each), 40884389871738(case) - Amount recalled
- 39341 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.
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.
Free recall alerts
Get alerted about new Medline Industries, LP recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.