Reported Jun 24, 2026 · Ongoing
MEDLINE Medical Procedure Kits labeled as: 1) D AND C PACK, Medline Kit Number/SKU DYNJ53973C; 2) PK CUST CV A&B…
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) D AND C PACKMedline Kit Number/SKU DYNJ53973C2) PK CUST CV A&B CABRINI COMedline Kit Number/SKU DYNJ60583C
- Lot codes and dates
6 of 6 products
Products covered by this recall Model / number Barcodes Product as published DYNJ53973C1019532700886440195327008865Medline Product Number/ : UDI/DI 10195327008864 (each), 40195327008865 (case), Lot Number 21KME435 DYNJ53973C1019532700886440195327008865Medline Product Number/ : UDI/DI 10195327008864 (each), 40195327008865 (case), Lot Number 21JMC247 DYNJ53973C1019532700886440195327008865Medline Product Number/ : UDI/DI 10195327008864 (each), 40195327008865 (case), Lot Number 21JMB678 DYNJ53973C1019532700886440195327008865Medline Product Number/ : UDI/DI 10195327008864 (each), 40195327008865 (case), Lot Number 21IMH919 DYNJ60583C1019532760558240195327605583Medline Product Number/ : UDI/DI 10195327605582 (each), 40195327605583 (case), Lot Number 24CBO389 DYNJ60583C1019532760558240195327605583Medline Product Number/ : UDI/DI 10195327605582 (each), 40195327605583 (case), Lot Number 24ABR872. - Amount recalled
- 168 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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