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
| Model / number | Barcodes | Product as published |
|---|---|---|
CDS980754T | 1019845912181440198459121815 | UDI/DI 10198459121814 (EA) 40198459121815 (CS), Lot Number 25EMD795 |
CDS982662Q | 1019532730679340195327306794 | UDI/DI 10195327306793 (EA) 40195327306794 (CS), Lot Number 25EBR237 |
CDS982662Q | 1019532730679340195327306794 | UDI/DI 10195327306793 (EA) 40195327306794 (CS), Lot Number 25EBP591 |
CDS982662Q | 1019532730679340195327306794 | UDI/DI 10195327306793 (EA) 40195327306794 (CS), Lot Number 25DBM353 |
CDS982662Q | 1019532730679340195327306794 | UDI/DI 10195327306793 (EA) 40195327306794 (CS), Lot Number 25CBL184 |
CDS982662Q | 1019532730679340195327306794 | UDI/DI 10195327306793 (EA) 40195327306794 (CS), Lot Number 25BBL633 |
CDS985344F | 1019532731256540195327312566 | UDI/DI 10195327312565 (EA) 40195327312566 (CS), Lot Number 25FBK918 |
CDS985344F | 1019532731256540195327312566 | UDI/DI 10195327312565 (EA) 40195327312566 (CS), Lot Number 25CBJ496 |
DYNJQ9041R | 1019845904308640198459043087 | UDI/DI 10198459043086 (EA) 40198459043087 (CS), Lot Number 25FBF371 |
DYNJQ9041R | 1019845904308640198459043087 | UDI/DI 10198459043086 (EA) 40198459043087 (CS), Lot Number 25EBK493 |
DYNJQ9041R | 1019845904308640198459043087 | UDI/DI 10198459043086 (EA) 40198459043087 (CS), Lot Number 25DBH895 |
DYNJ900244I | 1019532746492940195327464920 | UDI/DI 10195327464929 (EA) 40195327464920 (CS), Lot Number 25DBC272 |
DYNJ900244I | 1019532746492940195327464920 | UDI/DI 10195327464929 (EA) 40195327464920 (CS), Lot Number 25CBU642 |
DYNJ900244I | 1019532746492940195327464920 | UDI/DI 10195327464929 (EA) 40195327464920 (CS), Lot Number 25CBJ298 |
DYNJ900244I | 1019532746492940195327464920 | UDI/DI 10195327464929 (EA) 40195327464920 (CS), Lot Number 25BBU206 |
DYNJ901281I | 1019532769915440195327699155 | UDI/DI 10195327699154 (EA) 40195327699155 (CS), Lot Number 25FBA261 |
DYNJ901281I | 1019532769915440195327699155 | UDI/DI 10195327699154 (EA) 40195327699155 (CS), Lot Number 25CBN230 |
DYNJ901829T | 1019845923138440198459231385 | UDI/DI 10198459231384 (EA) 40198459231385 (CS), Lot Number 25FDB398 |
DYNJ901829T | 1019845923138440198459231385 | UDI/DI 10198459231384 (EA) 40198459231385 (CS), Lot Number 25DDA191 |
DYNJ901829T | 1019845923138440198459231385 | UDI/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.
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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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