Reported Apr 29, 2026 · Ongoing
Medline 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 Kits
81 of 81 products
| Model / number | Product as published |
|---|---|
CDS840228F | CATH LAB CDS |
DYNDH2104 | IR PACK |
DYNJT2164M | CARDIAC CATH PACK-LF |
DYNJT3078 | ANGIOGRAPHY TRAY |
DYNJT4190 | CATH PACK |
DYNJT5717 | ANGIO VASCULAR PACK |
DYNJ0381139R | HEART CATH PACK |
DYNJ04529L | CARDIAC CATH PACK |
DYNJ07955L | CUSTOM RADIOLOGY PACK |
DYNJ24619J | STVZ CARDIAC CATH PACK |
DYNJ24706D | CATH TRAY #2 |
DYNJ24802Q | CATH LAB PACK |
DYNJ30268K | CATH PACK |
DYNJ30927R | HEART CATHETERIZATION PACK |
DYNJ31944D | HEART CATH TRAY PACK-LF |
DYNJ33061D | CATH PACK-LF |
DYNJ34638K | CATH PACK |
DYNJ38120C | ANGIOGRAPHY DRAPE PACK |
DYNJ40904G | CATH PACK |
DYNJ41057D | CARDIAC CATH-LF |
- Lot codes and dates
361 of 361 products
Products covered by this recall # Barcodes Product as published 1 1088994277854640889942778547Lot Number: 25ALA420; 2) CDS840228F, UDI-DI: 10889942778546(each), 40889942778547(case) 2 1088994277854640889942778547Lot Number: 25CLA774; 3) CDS840228F, UDI-DI: 10889942778546(each), 40889942778547(case) 3 1019845927396440198459273965Lot Number: 24LLA038; 4) DYNDH2104, UDI-DI: 10198459273964(each), 40198459273965(case) 4 1019845900316540198459003166Lot Number: 25DBR609; 5) DYNJT2164M, UDI-DI: 10198459003165(each), 40198459003166(case) 5 1019845930514640198459305147Lot Number: 24JBT885; 6) DYNJT3078, UDI-DI: 10198459305146(each), 40198459305147(case) 6 1019845942823440198459428235Lot Number: 25DBN722; 7) DYNJT4190, UDI-DI: 10198459428234(each), 40198459428235(case) 7 1019845949668440198459496685Lot Number: 25HBA387; 8) DYNJT5717, UDI-DI: 10198459496684(each), 40198459496685(case) 8 1019845927601940198459276010Lot Number: 26ALA778; 9) DYNJ0381139R, UDI-DI: 10198459276019(each), 40198459276010(case) 9 1019845939146040198459391461Lot Number: 25JLA029; 10) DYNJ04529L, UDI-DI: 10198459391460(each), 40198459391461(case) 10 1088994262889640889942628897Lot Number: 25JLA312; 11) DYNJ07955L, UDI-DI: 10889942628896(each), 40889942628897(case) 11 1088994262889640889942628897Lot Number: 24HBM316; 12) DYNJ07955L, UDI-DI: 10889942628896(each), 40889942628897(case) 12 1019532729563940195327295630Lot Number: 23HBX895; 13) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case) 13 1019532729563940195327295630Lot Number: 23DBP876; 14) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case) 14 1019532729563940195327295630Lot Number: 23FBG933; 15) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case) 15 1019532729563940195327295630Lot Number: 24GBE563; 16) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case) 16 1019532729563940195327295630Lot Number: 24HBT787; 17) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case) 17 1019532729563940195327295630Lot Number: 24KBC564; 18) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case) 18 1019532729563940195327295630Lot Number: 24LBL445; 19) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case) 19 1019532729563940195327295630Lot Number: 25DBF355; 20) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case) 20 1088994229712240889942297123Lot Number: 25EBG106; 21) DYNJ24706D, UDI-DI: 10889942297122(each), 40889942297123(case) - Amount recalled
- 160883 units
This recall covers 39 products
The agency filed one notice per product. You are reading one of them; the other 38 are below.
26 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
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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