Botanical Be
Botanical Be appears in FDA public data with 3 recalls — including 3 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 1 compliance action on record. Its most recent recall (D-0225-2024, Class I) was initiated on October 20, 2023.
Summary
- Total Recalls
- 3 (3 Class I)
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 1
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| D-0225-2024 | Class I | Reumo Flex caplets, packaged in 30-count boxes, Manufactured by: Grupo Yepenza de Mexico, SA de CV, | October 20, 2023 |
| D-0224-2024 | Class I | Artri King Reforzado con Origa y Omega 3 tablets, packaged in 100-count bottles, Manufactured by: Pl | October 20, 2023 |
| D-0226-2024 | Class I | Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega N | October 20, 2023 |