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FDAFDA · Food and drugs·Recall number Z-2865-2026

STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530

Published August 12, 2026 · Recall initiated: June 8, 2026

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Stryker Corporation
Distributor
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.
Lot
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.
Risk classification
Class II
Area (FDA)
device
Country
United States

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