Reported Aug 12, 2026 · Ongoing · Updated Sep 16, 2026
STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530
Stryker Corporation
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: Stryker Corporation · 5900 Optical Ct · San Jose, CA · 95138-1400
Is this the product you have?
- STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530
- Lot codes and dates
GTIN 07613327061352Batch Numbers 24260FG224261FG224297FG224298FG224299FG224302FG224340FG224341FG225008FG225009FG225010FG225011FG225024FG225034FG225035FG225052FG225063FG225064FG225084FG225092FG225093FG225121FG225134FG225135FG225153FG225154FG225167FG225182FG225183FG225216FG225217FG225245FG225274FG2
- Amount recalled
- 11,857 Units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
There has been an increased amount in reported complaints consistently describing leaking from the handpiece 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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