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FDA (Device enforcement)Recalled 2026-06-08class ii

Stryker Corporation: STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530

Hazard

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

Details from the source

Reason for recall: There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. 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. Quantity: 11,857 Units Lot/code info: 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.

UPC codes

07613327061352

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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