BAPS SHAYONA Motichur Ladoo Sweet chickpea flour mini-pearls rolled into spheres Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047
Recalling firm: BAPS Shayona
Why it was recalled
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5 & #6.
The exact product
BAPS SHAYONA Motichur Ladoo Sweet chickpea flour mini-pearls rolled into spheres Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53160 Contains: Milk
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
02G0623 BEST BY 08/20/2023, 02G0623 BEST BY 8/20/2023, BEST BY 08/15/2023, 04F1423 BEST BY 7/29/2023 & 11F0823 BEST BY 7/23/2023
| Type | Code / value | Context |
|---|---|---|
| best by | 08/15/2023 | 02G0623 BEST BY 08/20/2023, 02G0623 BEST BY 8/20/2023, BEST BY 08/15/2023, 04F1423 BEST BY 7/29/2023 & 11F0823 BEST BY 7/23/2023 |
| best by | 08/20/2023 | 02G0623 BEST BY 08/20/2023, 02G0623 BEST BY 8/20/2023, BEST BY 08/15/2023, 04F1423 BEST BY 7/29/2023 & 11F0823 BEST BY 7/23/2023 |
| best by | 7/23/2023 | T BY 8/20/2023, BEST BY 08/15/2023, 04F1423 BEST BY 7/29/2023 & 11F0823 BEST BY 7/23/2023 |
| best by | 7/29/2023 | T BY 08/20/2023, 02G0623 BEST BY 8/20/2023, BEST BY 08/15/2023, 04F1423 BEST BY 7/29/2023 & 11F0823 BEST BY 7/23/2023 |
| best by | 8/20/2023 | 02G0623 BEST BY 08/20/2023, 02G0623 BEST BY 8/20/2023, BEST BY 08/15/2023, 04F1423 BEST BY 7/29/2023 & 11F0823 BEST BY 7/23/2023 |
Recall details
- Recall number
- F-0494-2024
- Event ID
- 92774
- FDA status
- Ongoing
- Initiated
- Jul 27, 2023
- Reported
- Dec 13, 2023
- Classified
- Dec 4, 2023
- Quantity
- 674 units
- Location
- Lilburn, GA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
Product was shipped to the following states: AL, FL, GA, NC, SC & TN
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.