Home › MEDTRONIC, INC. › SPRINTER® LEGEND

SPRINTER® LEGEND

MEDTRONIC, INC. · Model SPL37515X · UDI-DI 00763000877514

LOX Prescription

510(k) clearances

43,512

Adverse events (583 deaths)

121

Recalls

Facilities

Description

BALLOON SPL37515X SPR LEG RX US M

Recalls

Date	Firm	Reason
2022-06-24	Medtronic Inc	Luer has balloon diameter printed as "2.25mmx12mm" instead of the correct diameter, "2.5mmx12mm" as reflected on the product outer packaging.
2020-01-29	Abbott Vascular	Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29	Abbott Vascular	Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29	Abbott Vascular	Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29	Abbott Vascular	Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29	Abbott Vascular	Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29	Abbott Vascular	Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29	Abbott Vascular	Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29	Abbott Vascular	Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
2020-01-29	Abbott Vascular	Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.