WHY THIS PRODUCT IS LISTED
Other / see reason
Product contains the unapproved ingredient, picamilon.
Product description & recall reason
The recall record describes “Vanish V3”; the source reports: “Product contains the unapproved ingredient, picamilon.”
Based on the official recall record; packaging and sales claims have not been verified. Verify with the official source ↗
Identify the product
- Product description
- Vanish V3
- Brand
- Not supplied by this source
- Lot, batch, UPC & other codes
- XCA105620815
- Quantity
- 573 units
Where it came from & where it went
- Recalling firm
- ProSupps USA LLC
- Recalling firm address
- 2801 E Plano Pkwy; N/A; Plano; TX; 75074-7418; United States
- Product production / origin location
- Not supplied by this source
- Distribution — source wording
- US and Canada
States identified in the source
No specific states identified in the available distribution text.
State matching is derived from the source’s distribution wording, which may be incomplete. The recalling company’s address is not used as the distribution location.
A recalling firm’s address is not necessarily where the food was grown or manufactured. Distribution can change; check the official notice.
The dates, separated
- Recall initiated
- Aug 30, 2017
- Notice published
- Not supplied
- Enforcement report
- Oct 11, 2017
- Agency classification
- Sep 29, 2017
- Source termination date
- Feb 6, 2018
- Last retrieved here
- Sep 28, 2026
FDA’s enforcement status is historical and may not reflect the current recall lifecycle. A terminated recall does not certify a product as safe.
Record provenance & interpretation
- Source identifier
- F-3602-2017
- Agency event identifier
- 78043
- Status as supplied (not live status)
- Terminated
- Category assignment
- Inferred from product text; not an agency classification.
- State matching
- Official distribution wording; locations are extracted only from distribution evidence, not company addresses. Coverage may be incomplete.
- Source dataset date
- Sep 25, 2026