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?
73 of 73 products
| Model / number | Barcodes | Product as published |
|---|---|---|
CDS860237AF | 1019845923262640198459232627 | UDI/DI 10198459232626 (EA) 40198459232627 (CS), Lot Number 25FBK870 |
CDS860237AF | 1019845923262640198459232627 | UDI/DI 10198459232626 (EA) 40198459232627 (CS), Lot Number 25EBD110 |
CDS982128Q | 1019845900824540198459008246 | UDI/DI 10198459008245 (EA) 40198459008246 (CS), Lot Number 25EBC253 |
CDS982128Q | 1019845900824540198459008246 | UDI/DI 10198459008245 (EA) 40198459008246 (CS), Lot Number 25DBG393 |
CDS984338M | 1019845914810140198459148102 | UDI/DI 10198459148101 (EA) 40198459148102 (CS), Lot Number 25FBQ303 |
CDS984338M | 1019845914810140198459148102 | UDI/DI 10198459148101 (EA) 40198459148102 (CS), Lot Number 25EBD631 |
CDS984338M | 1019845914810140198459148102 | UDI/DI 10198459148101 (EA) 40198459148102 (CS), Lot Number 25DBM322 |
CDS984640I | 1019845931895540198459318956 | UDI/DI 10198459318955 (EA) 40198459318956 (CS), Lot Number 25DBT807 |
DYNJ0525321O | 1019845923690740198459236908 | UDI/DI 10198459236907 (EA) 40198459236908 (CS), Lot Number 25DMG099 |
DYNJ0525321O | 1019845923690740198459236908 | UDI/DI 10198459236907 (EA) 40198459236908 (CS), Lot Number 25CMJ006 |
DYNJ57640F | 1019845901111540198459011116 | UDI/DI 10198459011115 (EA) 40198459011116 (CS), Lot Number 25FDB347 |
DYNJ62594D | 1019845904976740198459049768 | UDI/DI 10198459049767 (EA) 40198459049768 (CS), Lot Number 25EBK539 |
DYNJ62594D | 1019845904976740198459049768 | UDI/DI 10198459049767 (EA) 40198459049768 (CS), Lot Number 25DBD145 |
DYNJ63392D | 1019845916450740198459164508 | UDI/DI 10198459164507 (EA) 40198459164508 (CS), Lot Number 25BLA967 |
DYNJ68187B | 1019845938208640198459382087 | UDI/DI 10198459382086 (EA) 40198459382087 (CS), Lot Number 25FMG440 |
DYNJ82368A | 1019845925807740198459258078 | UDI/DI 10198459258077 (EA) 40198459258078 (CS), Lot Number 25EMH020 |
DYNJ82368A | 1019845925807740198459258078 | UDI/DI 10198459258077 (EA) 40198459258078 (CS), Lot Number 25CMF917 |
DYNJ85261 | 1019532748341840195327483419 | UDI/DI 10195327483418 (EA) 40195327483419 (CS), Lot Number 25FBK331 |
DYNJ85261 | 1019532748341840195327483419 | UDI/DI 10195327483418 (EA) 40195327483419 (CS), Lot Number 25EBR783 |
DYNJ86178B | 1019845910480040198459104801 | UDI/DI 10198459104800 (EA) 40198459104801 (CS), Lot Number 25EBP320 |
- Amount recalled
- 4536 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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