FDAAugust 5, 2025device

Boston Scientific UroMax Ultra Kit, Material Numbers (UPN): 1. M0062251200, 2. M0062251210, 3. M0062251220, 4. M0062251230, 5. M0062251240, 6. M0062251260, 7. M0062251290, 8. M0062251300, 9. M0062251310. 10. M0062251350, 11. M0062251360, 12. M0062251370. (Urology)

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The Encore 26 Inflation Device is used with balloon dilation catheters to create and monitor pressure in the balloon and to deflate the balloon. An internal investigation determined that during use, foreign material particles could migrate from affected Encore 26 Inflation Devices into a balloon dilatation catheter.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

871472934127787147293412848714729341291871472934130787147293413148714729341338087147293413690871472934137608714729341383087147293413900871472930242108714729302438

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Boston Scientific UroMax Ultra Kit, Material Numbers (UPN): 1. M0062251200, 2. M0062251210, 3. M0062251220, 4. M0062251230, 5. M0062251240, 6. M0062251260, 7. M0062251290, 8. M0062251300, 9. M0062251310. 10. M0062251350, 11. M0062251360, 12. M0062251370. (Urology) — Recall Details · AllClear