Reported Jun 24, 2026 · Ongoing

MEDLINE Medical Procedure Kits labeled as

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?

89 of 89 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 23JBM539
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 23IBF088
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 23FBM203
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 22JBK233
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 22JBB115
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 22IBO304
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 22HBR331
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 22FBM460
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 22DBS093
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 22CBJ072
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 22BBX288
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 21LBU240
DYNJ67331B1019532701383740195327013838Medline Kit Number/ : UDI/DI 10195327013837 (each), 40195327013838 (case), Lot Number 21JBP452
DYNJ911589A1019845964610240198459646103Medline Kit Number/ : UDI/DI 10198459646102 (each), 40198459646103 (case), Lot Number 26CBD487
DYNJ36211D1088994288565740889942885658Medline Kit Number/ : UDI/DI 10889942885657 (each), 40889942885658 (case), Lot Number 24EBB811
DYNJ36211D1088994288565740889942885658Medline Kit Number/ : UDI/DI 10889942885657 (each), 40889942885658 (case), Lot Number 24ABV035
DYNJ36211D1088994288565740889942885658Medline Kit Number/ : UDI/DI 10889942885657 (each), 40889942885658 (case), Lot Number 23LBG394
DYNJ36211D1088994288565740889942885658Medline Kit Number/ : UDI/DI 10889942885657 (each), 40889942885658 (case), Lot Number 23KBA664
DYNJ36211D1088994288565740889942885658Medline Kit Number/ : UDI/DI 10889942885657 (each), 40889942885658 (case), Lot Number 23HBC987
DYNJ36211D1088994288565740889942885658Medline Kit Number/ : UDI/DI 10889942885657 (each), 40889942885658 (case), Lot Number 23GBQ638
Amount recalled
4801 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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By hazard

Other recalls from Medline Industries, LP

36 in total.

Where it was distributed

All recall categories · Browse the whole archive

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:54 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.