Stryker Corporation recalls STRYKER PKG.
- Recalling company
- Stryker Corporation
- Product
- STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530
- Reason
- There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jun 8, 2026
- Reported
- Aug 12, 2026
- Distribution
- Worldwide distribution - 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.
- Status
- Ongoing
- Quantity
- 11,857 Units
- Lot / codes
- GTIN 07613327061352, Batch Numbers 24260FG2, 24261FG2, 24297FG2, 24298FG2, 24299FG2, 24302FG2, 24340FG2, 24341FG2, 25008FG2, 25009FG2, 25010FG2, 25011FG2, 25024FG2, 25034FG2, 25035FG2, 25052FG2, 25063FG2, 25064FG2, 25084FG2, 25092FG2, 25093FG2, 25121FG2, 25134FG2, 25135FG2, 25153FG2, 25154FG2, 25167FG2, 25182FG2, 25183FG2, 25216FG2, 25217FG2, 25245FG2, 25274FG2.
- Company location
- San Jose, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2865-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2865-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.