Reported Oct 21, 2026 · Ongoing · Updated Oct 26, 2026

Medline surgical 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?

34 of 34 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ909020B1019845915921340198459159214Medline product number/ , UDI/DI 10198459159213 (each) 40198459159214 (case), Lot number 26AMF311
DYNJ909020B1019845915921340198459159214Medline product number/ , UDI/DI 10198459159213 (each) 40198459159214 (case), Lot number 25JMD500
DYNJ909020B1019845915921340198459159214Medline product number/ , UDI/DI 10198459159213 (each) 40198459159214 (case), Lot number 25DMJ849
DYNJ909020B1019845915921340198459159214Medline product number/ , UDI/DI 10198459159213 (each) 40198459159214 (case), Lot number 25CMD823
DYNJ909020B1019845915921340198459159214Medline product number/ , UDI/DI 10198459159213 (each) 40198459159214 (case), Lot number 25BMG250
DYNJ909020B1019845915921340198459159214Medline product number/ , UDI/DI 10198459159213 (each) 40198459159214 (case), Lot number 24LMG633
DYNJ909020A1019532766576040195327665761Medline product number/ , UDI/DI 10195327665760 (each) 40195327665761 (case), Lot number 24KMB736
DYNJ909020A1019532766576040195327665761Medline product number/ , UDI/DI 10195327665760 (each) 40195327665761 (case), Lot number 24JMD634
DYNJ909020A1019532766576040195327665761Medline product number/ , UDI/DI 10195327665760 (each) 40195327665761 (case), Lot number 24IMD605
DYNJ42922C1019348933501940193489335010Medline product number/ , UDI/DI 10193489335019 (each) 40193489335010 (case), Lot number 24HBT243
DYNJ42922C1019348933501940193489335010Medline product number/ , UDI/DI 10193489335019 (each) 40193489335010 (case), Lot number 24HBD143
DYNJ909020A1019532766576040195327665761Medline product number/ , UDI/DI 10195327665760 (each) 40195327665761 (case), Lot number 24GMG103
DYNJ909020A1019532766576040195327665761Medline product number/ , UDI/DI 10195327665760 (each) 40195327665761 (case), Lot number 24DMI379
DYNJ42922C1019348933501940193489335010Medline product number/ , UDI/DI 10193489335019 (each) 40193489335010 (case), Lot number 24CBJ928
DYNJ9090201019532724867340195327248674Medline product number/ , UDI/DI 10195327248673 (each) 40195327248674 (case), Lot number 24BME929
DYNJ657061019348928490440193489284905Medline product number/ , UDI/DI 10193489284904 (each) 40193489284905 (case), Lot number 24AMF210
DYNJ9090201019532724867340195327248674Medline product number/ , UDI/DI 10195327248673 (each) 40195327248674 (case), Lot number 24AMD338
DYNJ9090201019532724867340195327248674Medline product number/ , UDI/DI 10195327248673 (each) 40195327248674 (case), Lot number 23LME666
DYNJ9090201019532724867340195327248674Medline product number/ , UDI/DI 10195327248673 (each) 40195327248674 (case), Lot number 23LMB230
DYNJ9090201019532724867340195327248674Medline product number/ , UDI/DI 10195327248673 (each) 40195327248674 (case), Lot number 23KMF895
Amount recalled
620 kits

This recall covers 11 products

The agency filed one notice per product. You are reading one of them; the other 10 are below.

Where it was sold

  • Nationwide

Why it was recalled

Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

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 Nov 4, 1:50 AM 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.