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FDA
Food and Drug Administration · Recall Z-2862-2026 · Jun 8, 2026

STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600

Stryker Corporation

The hazard

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

The remedy

Follow FDA guidance

About this recall

STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model GTIN 07613327061499Model Batch Numbers: 24262FG2Model 24263FG2Model 24264FG2Model 24266FG2Model 24267FG2Model 24268FG2Model 24269FG2Model 24283FG2Model 24284FG2Model 24286FG2Model 24287FG2Model 24288FG2Model 24289FG2Model 24290FG2Model 24291FG2Model 24292FG2Model 24293FG2Model 24294FG2Model 24295FG2Model 24296FG2Model 24298FG2Model 24299FG2Model 24302FG2Model 24303FG2UPC 07613327061499

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.