FDAMay 8, 2025device

Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311 PRES1045CPKPLT 00810068567663 PRES1245CPKPLT 00810068567694 PRES1445CPKPLT 00810068567724 PRES0103CXPPLT 00810068567304 PRES2512CXPPLT 00810068567397 PRES0258CXPPLT 00810068567380 PRES0212CXPPLT 00810068567373 PRES0204CXPPLT 00...

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

The hazard

Due to radiopaque (RO) marker was not visible during angiography and it was determined that the RO marker was not manufactured to specification.

What to do

FDA enforcement status: Ongoing

Brands named

balt

UPCs

008100685673110081006856766300810068567694008100685677240081006856730400810068567397008100685673800081006856737300810068567342008100685673590081006856736600810068567441

Recall history

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

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