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

Products covered by this recall
Model / numberProduct as published
CDS840228FCATH LAB CDS
DYNDH2104IR PACK
DYNJT2164MCARDIAC CATH PACK-LF
DYNJT3078ANGIOGRAPHY TRAY
DYNJT4190CATH PACK
DYNJT5717ANGIO VASCULAR PACK
DYNJ0381139RHEART CATH PACK
DYNJ04529LCARDIAC CATH PACK
DYNJ07955LCUSTOM RADIOLOGY PACK
DYNJ24619JSTVZ CARDIAC CATH PACK
DYNJ24706DCATH TRAY #2
DYNJ24802QCATH LAB PACK
DYNJ30268KCATH PACK
DYNJ30927RHEART CATHETERIZATION PACK
DYNJ31944DHEART CATH TRAY PACK-LF
DYNJ33061DCATH PACK-LF
DYNJ34638KCATH PACK
DYNJ38120CANGIOGRAPHY DRAPE PACK
DYNJ40904GCATH PACK
DYNJ41057DCARDIAC CATH-LF
Lot codes and dates

361 of 361 products

Products covered by this recall
#BarcodesProduct as published
11088994277854640889942778547Lot Number: 25ALA420; 2) CDS840228F, UDI-DI: 10889942778546(each), 40889942778547(case)
21088994277854640889942778547Lot Number: 25CLA774; 3) CDS840228F, UDI-DI: 10889942778546(each), 40889942778547(case)
31019845927396440198459273965Lot Number: 24LLA038; 4) DYNDH2104, UDI-DI: 10198459273964(each), 40198459273965(case)
41019845900316540198459003166Lot Number: 25DBR609; 5) DYNJT2164M, UDI-DI: 10198459003165(each), 40198459003166(case)
51019845930514640198459305147Lot Number: 24JBT885; 6) DYNJT3078, UDI-DI: 10198459305146(each), 40198459305147(case)
61019845942823440198459428235Lot Number: 25DBN722; 7) DYNJT4190, UDI-DI: 10198459428234(each), 40198459428235(case)
71019845949668440198459496685Lot Number: 25HBA387; 8) DYNJT5717, UDI-DI: 10198459496684(each), 40198459496685(case)
81019845927601940198459276010Lot Number: 26ALA778; 9) DYNJ0381139R, UDI-DI: 10198459276019(each), 40198459276010(case)
91019845939146040198459391461Lot Number: 25JLA029; 10) DYNJ04529L, UDI-DI: 10198459391460(each), 40198459391461(case)
101088994262889640889942628897Lot Number: 25JLA312; 11) DYNJ07955L, UDI-DI: 10889942628896(each), 40889942628897(case)
111088994262889640889942628897Lot Number: 24HBM316; 12) DYNJ07955L, UDI-DI: 10889942628896(each), 40889942628897(case)
121019532729563940195327295630Lot Number: 23HBX895; 13) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case)
131019532729563940195327295630Lot Number: 23DBP876; 14) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case)
141019532729563940195327295630Lot Number: 23FBG933; 15) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case)
151019532729563940195327295630Lot Number: 24GBE563; 16) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case)
161019532729563940195327295630Lot Number: 24HBT787; 17) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case)
171019532729563940195327295630Lot Number: 24KBC564; 18) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case)
181019532729563940195327295630Lot Number: 24LBL445; 19) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case)
191019532729563940195327295630Lot Number: 25DBF355; 20) DYNJ24619J, UDI-DI: 10195327295639(each), 40195327295630(case)
201088994229712240889942297123Lot 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:33 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.