Reported Jun 24, 2026 · Ongoing
MEDLINE Medical Procedure Kits labeled as: 1) CAROTID NEURO PACK, Medline Kit Number/SKU DYNJ44926G; 2) VP SHUNT CDS,…
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
1) CAROTID NEURO PACKMedline Kit Number/SKU DYNJ44926G2) VP SHUNT CDSMedline Kit Number/SKU CDS983800J3) VP SHUNT CDSMedline Kit Number/SKU CDS983800K
- Lot codes and dates
16 of 16 products
Products covered by this recall Model / number Barcodes Product as published DYNJ44926G1019348976655440193489766555Medline Kit Number/ : UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 24EBH848 DYNJ44926G1019348976655440193489766555Medline Kit Number/ : UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 24DBK995 DYNJ44926G1019348976655440193489766555Medline Kit Number/ : UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 23JBP023 DYNJ44926G1019348976655440193489766555Medline Kit Number/ : UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 23HBR067 DYNJ44926G1019348976655440193489766555Medline Kit Number/ : UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 23FBM330 DYNJ44926G1019348976655440193489766555Medline Kit Number/ : UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 23EBK061 DYNJ44926G1019348976655440193489766555Medline Kit Number/ : UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 22JBG042 DYNJ44926G1019348976655440193489766555Medline Kit Number/ : UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 22GBH864 DYNJ44926G1019348976655440193489766555Medline Kit Number/ : UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 22DBT571 CDS983800J1019532768466240195327684663Medline Kit Number/ : UDI/DI 10195327684662 (each), 40195327684663 (case), Lot Number 25DMJ438 CDS983800J1019532768466240195327684663Medline Kit Number/ : UDI/DI 10195327684662 (each), 40195327684663 (case), Lot Number 25CMH178 CDS983800J1019532768466240195327684663Medline Kit Number/ : UDI/DI 10195327684662 (each), 40195327684663 (case), Lot Number 24IME720 CDS983800J1019532768466240195327684663Medline Kit Number/ : UDI/DI 10195327684662 (each), 40195327684663 (case), Lot Number 24HMG912 CDS983800K1019845951897340198459518974Medline Kit Number/ : UDI/DI 10198459518973 (each), 40198459518974 (case), Lot Number 26CMC503 CDS983800K1019845951897340198459518974Medline Kit Number/ : UDI/DI 10198459518973 (each), 40198459518974 (case), Lot Number 26AMB047 CDS983800K1019845951897340198459518974Medline Kit Number/ : UDI/DI 10198459518973 (each), 40198459518974 (case), Lot Number 25JME109. - Amount recalled
- 342 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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