Stryker Strykeflow Suction/Irrigator PS Recall
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Stryker Corporation is recalling 589 units of STRYKEFLOW SUCTION/IRRIGATOR PS devices due to reports of leaking from the handpiece.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 20, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, MedicalDevices.
What Happened
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Which Products Are Affected
STRYKER PKG., STRYKEFLOW SUCTION/IRRIGATOR PS, Catalog Number 0250070540. GTIN 0761332706146. Batch Numbers: 24297FG2, 24306FG2, 24344FG2, 25007FG2, 25065FG2, 25091FG2, 25168FG2. 589 units. Worldwide distribution including US Nationwide and the countries of Australia, Brazil, Canada, Chile, France, Germany, Indonesia, Italy, Mexico, Netherlands, New Zealand, Philippines, South Korea, Spain, Sweden, Switzerland, Taiwan, United Kingdom. Recall number Z-2866-2026. Class II recall.
What You Should Do
Contact the recalling firm for additional information regarding the recall.
Why This Matters
This Class II recall involves a medical device distributed nationwide and internationally.
Source
FDA recall number Z-2866-2026, report date 20260812.
Original source: FDA Official Notice ↗
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