Reported Jan 21, 2026 · Ongoing

Medline medical procedure 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?

32 of 32 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS980754T1019845912181440198459121815UDI/DI 10198459121814 (EA) 40198459121815 (CS), Lot Number 25EMD795
CDS982662Q1019532730679340195327306794UDI/DI 10195327306793 (EA) 40195327306794 (CS), Lot Number 25EBR237
CDS982662Q1019532730679340195327306794UDI/DI 10195327306793 (EA) 40195327306794 (CS), Lot Number 25EBP591
CDS982662Q1019532730679340195327306794UDI/DI 10195327306793 (EA) 40195327306794 (CS), Lot Number 25DBM353
CDS982662Q1019532730679340195327306794UDI/DI 10195327306793 (EA) 40195327306794 (CS), Lot Number 25CBL184
CDS982662Q1019532730679340195327306794UDI/DI 10195327306793 (EA) 40195327306794 (CS), Lot Number 25BBL633
CDS985344F1019532731256540195327312566UDI/DI 10195327312565 (EA) 40195327312566 (CS), Lot Number 25FBK918
CDS985344F1019532731256540195327312566UDI/DI 10195327312565 (EA) 40195327312566 (CS), Lot Number 25CBJ496
DYNJQ9041R1019845904308640198459043087UDI/DI 10198459043086 (EA) 40198459043087 (CS), Lot Number 25FBF371
DYNJQ9041R1019845904308640198459043087UDI/DI 10198459043086 (EA) 40198459043087 (CS), Lot Number 25EBK493
DYNJQ9041R1019845904308640198459043087UDI/DI 10198459043086 (EA) 40198459043087 (CS), Lot Number 25DBH895
DYNJ900244I1019532746492940195327464920UDI/DI 10195327464929 (EA) 40195327464920 (CS), Lot Number 25DBC272
DYNJ900244I1019532746492940195327464920UDI/DI 10195327464929 (EA) 40195327464920 (CS), Lot Number 25CBU642
DYNJ900244I1019532746492940195327464920UDI/DI 10195327464929 (EA) 40195327464920 (CS), Lot Number 25CBJ298
DYNJ900244I1019532746492940195327464920UDI/DI 10195327464929 (EA) 40195327464920 (CS), Lot Number 25BBU206
DYNJ901281I1019532769915440195327699155UDI/DI 10195327699154 (EA) 40195327699155 (CS), Lot Number 25FBA261
DYNJ901281I1019532769915440195327699155UDI/DI 10195327699154 (EA) 40195327699155 (CS), Lot Number 25CBN230
DYNJ901829T1019845923138440198459231385UDI/DI 10198459231384 (EA) 40198459231385 (CS), Lot Number 25FDB398
DYNJ901829T1019845923138440198459231385UDI/DI 10198459231384 (EA) 40198459231385 (CS), Lot Number 25DDA191
DYNJ901829T1019845923138440198459231385UDI/DI 10198459231384 (EA) 40198459231385 (CS), Lot Number 25BDB095
Amount recalled
1457 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

  • Nationwide

Why it was recalled

Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) 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.

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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, 5:38 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.