FDAApril 22, 2026device

RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U 28-N4-32-164-28U 28-N4-32-164-32U 28-N4-32-209-28U 28-N4-32-209-32U 28-N4-32-259-32U 28-N4-34-109-34U 28-N4-34-154-30U 28-N4-34-154-34U 28-N4-34-209-30U 28-N4-34-209-34U 28-N4-34-259-34U 28-N4-36-109-36U 28-N...

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

The hazard

Labeling update concerning proximal clasp disconnection from the outer control tube which may prevent stent graft from being released from the delivery system.

What to do

FDA enforcement status: Ongoing

Brands named

bolton medicalbolton

UPCs

008435761504610084357615095900843576150591008435761510550084357615072000843576150850008435761504780084357615096600843576150607008435761510620084357615073700843576150867

Recall history

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

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