Reported Jun 24, 2026 · Ongoing

MEDLINE Medical Procedure Kits labeled as CH OPEN HEART, ADULT CARDIAC KIT, AHT CVOR CABG, APH EMERGENCY OPEN HEART…

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 Medical Procedure Kits labeled as CH OPEN HEART, ADULT CARDIAC KIT, AHT CVOR CABG, APH EMERGENCY OPEN HEART PACK, Etc. (see recall documents for a full list of products)
Lot codes and dates

293 of 293 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS983773G1019348934424040193489344241Medline Kit Number/ : UDI/DI 10193489344240 (each), 40193489344241 (case), Lot Number 21ABD933
CDS983773I1019348984712340193489847124Medline Kit Number/ : UDI/DI 10193489847123 (each), 40193489847124 (case), Lot Number 22IBJ338
CDS983773I1019348984712340193489847124Medline Kit Number/ : UDI/DI 10193489847123 (each), 40193489847124 (case), Lot Number 22EBL456
CDS983773I1019348984712340193489847124Medline Kit Number/ : UDI/DI 10193489847123 (each), 40193489847124 (case), Lot Number 22EBL231
CDS983773I1019348984712340193489847124Medline Kit Number/ : UDI/DI 10193489847123 (each), 40193489847124 (case), Lot Number 22BBW955
CDS983773I1019348984712340193489847124Medline Kit Number/ : UDI/DI 10193489847123 (each), 40193489847124 (case), Lot Number 22ABC123
CDS983773I1019348984712340193489847124Medline Kit Number/ : UDI/DI 10193489847123 (each), 40193489847124 (case), Lot Number 21IBM442
CDS983773I1019348984712340193489847124Medline Kit Number/ : UDI/DI 10193489847123 (each), 40193489847124 (case), Lot Number 21IBI539
CDS983773I1019348984712340193489847124Medline Kit Number/ : UDI/DI 10193489847123 (each), 40193489847124 (case), Lot Number 21FBT730
CDS983773I1019348984712340193489847124Medline Kit Number/ : UDI/DI 10193489847123 (each), 40193489847124 (case), Lot Number 21EBA066
CDS983773I1019348984712340193489847124Medline Kit Number/ : UDI/DI 10193489847123 (each), 40193489847124 (case), Lot Number 21CBW872
CDS983773J1019532723361740195327233618Medline Kit Number/ : UDI/DI 10195327233617 (each), 40195327233618 (case), Lot Number 23HBV936
CDS983773J1019532723361740195327233618Medline Kit Number/ : UDI/DI 10195327233617 (each), 40195327233618 (case), Lot Number 23HBL135
CDS983773J1019532723361740195327233618Medline Kit Number/ : UDI/DI 10195327233617 (each), 40195327233618 (case), Lot Number 23HBH924
CDS983773J1019532723361740195327233618Medline Kit Number/ : UDI/DI 10195327233617 (each), 40195327233618 (case), Lot Number 23GBT133
CDS983773J1019532723361740195327233618Medline Kit Number/ : UDI/DI 10195327233617 (each), 40195327233618 (case), Lot Number 23GBD523
CDS983773J1019532723361740195327233618Medline Kit Number/ : UDI/DI 10195327233617 (each), 40195327233618 (case), Lot Number 23ABM749
CDS983773J1019532723361740195327233618Medline Kit Number/ : UDI/DI 10195327233617 (each), 40195327233618 (case), Lot Number 22JBH775
DYNJ39755A1019348967023340193489670234Medline Kit Number/ : UDI/DI 10193489670233 (each), 40193489670234 (case), Lot Number 24EDB118
DYNJ39755A1019348967023340193489670234Medline Kit Number/ : UDI/DI 10193489670233 (each), 40193489670234 (case), Lot Number 24DDC044
Amount recalled
168968 units

This recall covers 64 products

The agency filed one notice per product. You are reading one of them; the other 63 are below.

51 more are in the archive.

Where it was sold

Why it was recalled

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

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, 5:40 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.