FDA Drug recall D-0226-2024
Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal…
- FDA Drug
- Class I
- ongoing
- Published 2023-12-06
On 2023-12-06 the FDA classified a Class I recall of Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal… by Botanical Be, citing marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0226-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2023-10-20 |
| Published | 2023-12-06 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Botanical Be |
| Distribution | US |
Product
Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265
Reason
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Identifiers
| upc | 0736640810265 |
|---|---|
| code_info | All lots, exp 12/12/2024 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0226-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.