Reported Jul 29, 2026 · Ongoing

Medline medical convenience 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?

35 of 35 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ65065A1019348931724440193489317245Medline Kit , UDI/DI 10193489317244 (each) 40193489317245 (case), Lot Number 24KMI926
DYNJ65065A1019348931724440193489317245Medline Kit , UDI/DI 10193489317244 (each) 40193489317245 (case), Lot Number 25BMI009
DYNJ65065A1019348931724440193489317245Medline Kit , UDI/DI 10193489317244 (each) 40193489317245 (case), Lot Number 25DME458
DYNJ65065A1019348931724440193489317245Medline Kit , UDI/DI 10193489317244 (each) 40193489317245 (case), Lot Number 25FMC143
DYNJ65066B1019348931718340193489317184Medline Kit , UDI/DI 10193489317183 (each) 40193489317184 (case), Lot Number 24KME109
DYNJ65066B1019348931718340193489317184Medline Kit , UDI/DI 10193489317183 (each) 40193489317184 (case), Lot Number 24LMD416
DYNJ65066B1019348931718340193489317184Medline Kit , UDI/DI 10193489317183 (each) 40193489317184 (case), Lot Number 25BMB162
DYNJ65066B1019348931718340193489317184Medline Kit , UDI/DI 10193489317183 (each) 40193489317184 (case), Lot Number 25DMB403
DYNJ65066B1019348931718340193489317184Medline Kit , UDI/DI 10193489317183 (each) 40193489317184 (case), Lot Number 25DMK347
DYNJ65066B1019348931718340193489317184Medline Kit , UDI/DI 10193489317183 (each) 40193489317184 (case), Lot Number 25FMA695
DYNJ907718B1019532767180840195327671809Medline Kit , UDI/DI 10195327671808 (each) 40195327671809 (case), Lot Number 25ABJ808
DYNJ907718B1019532767180840195327671809Medline Kit , UDI/DI 10195327671808 (each) 40195327671809 (case), Lot Number 25ABM644
DYNJ907718B1019532767180840195327671809Medline Kit , UDI/DI 10195327671808 (each) 40195327671809 (case), Lot Number 25BBT262
DYNJ907732C1019532767172340195327671724Medline Kit , UDI/DI 10195327671723 (each) 40195327671724 (case), Lot Number 24LBD661
DYNJ907732C1019532767172340195327671724Medline Kit , UDI/DI 10195327671723 (each) 40195327671724 (case), Lot Number 25ABP134
DYNJ907732C1019532767172340195327671724Medline Kit , UDI/DI 10195327671723 (each) 40195327671724 (case), Lot Number 25BBS412
DYNJ907732C1019532767172340195327671724Medline Kit , UDI/DI 10195327671723 (each) 40195327671724 (case), Lot Number 25DBS673
DYNJ907732C1019532767172340195327671724Medline Kit , UDI/DI 10195327671723 (each) 40195327671724 (case), Lot Number 25FBS372
DYNJ907984C1019845913097740198459130978Medline Kit , UDI/DI 10198459130977 (each) 40198459130978 (case), Lot Number 25CBO351
DYNJ907987D1019845912988940198459129880Medline Kit , UDI/DI 10198459129889 (each) 40198459129880 (case), Lot Number 24LBO744
Amount recalled
1601 units

This recall covers 18 products

The agency filed one notice per product. You are reading one of them; the other 17 are below.

5 more are in the archive.

Where it was sold

Why it was recalled

Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Medline Industries, LP recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:33 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.