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 / number Barcodes Product 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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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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