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?

165 of 165 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS860235L1019845925866440198459258665UDI/DI 10198459258664 (EA)40198459258665 (CS), Kit Lot Number 25EMH913
CDS860235L1019845925866440198459258665UDI/DI 10198459258664 (EA)40198459258665 (CS), Kit Lot Number 25EMC376
CDS860235L1019845925866440198459258665UDI/DI 10198459258664 (EA)40198459258665 (CS), Kit Lot Number 25CMJ688
CDS860235L1019845925866440198459258665UDI/DI 10198459258664 (EA)40198459258665 (CS), Kit Lot Number 25CME476
CDS930223M1019845928260740198459282608UDI/DI 10198459282607 (EA)40198459282608 (CS), Kit Lot Number 25EBM987
CDS930223M1019845928260740198459282608UDI/DI 10198459282607 (EA)40198459282608 (CS), Kit Lot Number 25CBT666
CDS983678K1019532757224240195327572243UDI/DI 10195327572242 (EA)40195327572243 (CS), Kit Lot Number 25FBP815
CDS983678K1019532757224240195327572243UDI/DI 10195327572242 (EA)40195327572243 (CS), Kit Lot Number 25EBN002
CDS983678K1019532757224240195327572243UDI/DI 10195327572242 (EA)40195327572243 (CS), Kit Lot Number 25CBN212
CDS983679K1019532764151140195327641512UDI/DI 10195327641511 (EA)40195327641512 (CS), Kit Lot Number 25FBN760
CDS983679K1019532764151140195327641512UDI/DI 10195327641511 (EA)40195327641512 (CS), Kit Lot Number 25EBD329
CDS983679K1019532764151140195327641512UDI/DI 10195327641511 (EA)40195327641512 (CS), Kit Lot Number 25DBN040
CDS983679K1019532764151140195327641512UDI/DI 10195327641511 (EA)40195327641512 (CS), Kit Lot Number 25DBK313
CDS983679K1019532764151140195327641512UDI/DI 10195327641511 (EA)40195327641512 (CS), Kit Lot Number 25CBE452
CDS983752M1019532725585540195327255856UDI/DI 10195327255855 (EA)40195327255856 (CS), Kit Lot Number 25DMH793
CDS983752M1019532725585540195327255856UDI/DI 10195327255855 (EA)40195327255856 (CS), Kit Lot Number 25DMC405
CDS984016B1019532719107840195327191079UDI/DI 10195327191078 (EA)40195327191079 (CS), Kit Lot Number 25EBN676
CDS984016B1019532719107840195327191079UDI/DI 10195327191078 (EA)40195327191079 (CS), Kit Lot Number 25DBO816
CDS984016B1019532719107840195327191079UDI/DI 10195327191078 (EA)40195327191079 (CS), Kit Lot Number 25CBJ724
CDS984016B1019532719107840195327191079UDI/DI 10195327191078 (EA)40195327191079 (CS), Kit Lot Number 25BBK265
Amount recalled
41432 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.

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, 6:19 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.