FDAMay 8, 2025device

Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851 OPTI0258BLK 00810068568929 OPTI0212BLK 00810068568912 OPTI0206BLK 00810068568905 OPTI0310BLK 00810068568943 OPTI0320BLK 00810068568950 OPTI0151HSS10 00818053026614 OPTI0152HSS10 ...

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

008100685688750081006856888200810068568851008100685689290081006856891200810068568905008100685689430081006856895000818053025419008180530252800081805302530300818053025327

Recall history

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

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Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851 OPTI0258BLK 00810068568929 OPTI0212BLK 00810068568912 OPTI0206BLK 00810068568905 OPTI0310BLK 00810068568943 OPTI0320BLK 00810068568950 OPTI0151HSS10 00818053026614 OPTI0152HSS10 ... — Recall Details · AllClear