FDA device facilities in ME

7 registered medical-device facilities with FDA recall history in ME.

• Abbott Diagnostics Scarborough, Inc. FEI 3017662853
• Abbott Diagnostics Scarborough, Inc. FEI 1221359
• Abbott Diagnostics Scarborough, Inc. FEI 3029059580
• Advanced Instruments, LLC FEI 1221020
• FHC, INC. FEI 3002250546
• MOLNLYCKE MANUFACTURING US, LLC FEI 3010099071
• Molnlycke Manufacturing US, LLC FEI 3000719717

Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. We restate the public record only — measured facts, never risk verdicts.