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 PACK
    • Medline Kit Number/SKU DYNJ44926G
    • 2) VP SHUNT CDS
    • Medline Kit Number/SKU CDS983800J
    • 3) VP SHUNT CDS
    • Medline Kit Number/SKU CDS983800K
Lot codes and dates

16 of 16 products

Products covered by this recall
Model / numberBarcodesProduct 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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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:35 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.