Boulla LLC

FDA Regulatory Profile

Boulla LLC appears in FDA public data with 4 recalls — including 4 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0084-2025, Class I) was initiated on November 4, 2024.

Summary

Total Recalls
4 (4 Class I)
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-0084-2025Class IPeakMax Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: PeakMax, San FraNovember 4, 2024
D-0083-2025Class IVitalityXtra Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: VitalityXtrNovember 4, 2024
D-0085-2025Class IZoomMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZoomMax, 2108 N St. SacramenNovember 4, 2024
D-0086-2025Class IZapMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZapMax, 2108 N St. SacramentoNovember 4, 2024