Report cards › Food › Ancel Products Inc
ANCEL
CSWH grade C (61)
Method v1.0 (how we grade), based on the records below; exact score 60.7143.
| Indicator | Grade | What we found |
|---|---|---|
| Recalls (40%) | A (100) | No recalls found Oct 28, 2021 to Oct 28, 2026. For current recalls see FDA and USDA. |
| Ingredients (40%) | F (2) | Tier A: 2 of 7 products (FD&C Red No. 3) · F (0) (25%) Tier B: 4 of 7 products (FD&C Red No. 40, FD&C Yellow No. 6) · F (5) (15%) · products |
| FDA warning letters (20%) | A (100) | None found to the owner Oct 28, 2021 to Oct 28, 2026. |
Shown, not graded: recall reasons (none) · IARC notes (0 products) · FDA dye pledge: none on FDA's tracker.
Recalls, Oct 28, 2021 to Oct 28, 2026
No FDA recall matched to this brand.
Store-brand and co-packer recalls count on a brand only when a UPC in the recall matches one of its products.
Ingredients on our watch list
FD&C Red No. 3 Tier A in 2 of 7 products
- FDA order revoking the listing of FD&C Red No. 3 for food (90 FR 4628, 2025-01-16; stay lifted and dates confirmed, 91 FR 50475, 2026-08-05): revoked for food by FDA, effective Jan 15, 2027.
- California AB 418 (2023), the California Food Safety Act, Stats. 2023 ch. 328, Health and Safety Code § 109025: banned in food by state law (CA), effective Jan 1, 2027.
- West Virginia HB 2354 (2025), W. Va. Code § 16-7-2(b)(7): banned in food by state law (WV), effective Jan 1, 2028. Under court challenge (enforcement blocked for now): International Association of Color Manufacturers v. Singh.
- Texas SB 25, 89th Legislature (2025), Health and Safety Code § 431.0815 (warning label), § 431.0815(a)(32): warning label required by state law (TX), effective Jan 1, 2027. Under court challenge: American Beverage Association v. Paxton.
FD&C Red No. 40 Tier B in 4 of 7 products
- HHS/FDA phase-out of petroleum-based food dyes (announced 2025-04-22; voluntary industry pledges, no rule): FDA phase-out target, effective Dec 31, 2027.
- Texas SB 25, 89th Legislature (2025), Health and Safety Code § 431.0815 (warning label), § 431.0815(a)(34): warning label required by state law (TX), effective Jan 1, 2027. Under court challenge: American Beverage Association v. Paxton.
- West Virginia HB 2354 (2025), W. Va. Code § 16-7-2(b)(7): banned in food by state law (WV), effective Jan 1, 2028. Under court challenge (enforcement blocked for now): International Association of Color Manufacturers v. Singh.
FD&C Yellow No. 6 Tier B in 2 of 7 products
- HHS/FDA phase-out of petroleum-based food dyes (announced 2025-04-22; voluntary industry pledges, no rule): FDA phase-out target, effective Dec 31, 2027.
- Texas SB 25, 89th Legislature (2025), Health and Safety Code § 431.0815 (warning label), § 431.0815(a)(44): warning label required by state law (TX), effective Jan 1, 2027. Under court challenge: American Beverage Association v. Paxton.
- West Virginia HB 2354 (2025), W. Va. Code § 16-7-2(b)(7): banned in food by state law (WV), effective Jan 1, 2028. Under court challenge (enforcement blocked for now): International Association of Color Manufacturers v. Singh.
Products (4)
- ANCEL, GUAVA PASTE · UPC 74566131386 · FoodData Central record of Oct 28, 2021
A FD&C Red No. 3 ("fd and c red no 3"); B FD&C Red No. 40 ("fd and c red no 40"); B FD&C Yellow No. 6 ("fd and c yellow no 6") · Report an error - ANCEL, GUAVA PASTE WITH JELLY CENTER · UPC 74566131409 · FoodData Central record of Oct 28, 2021
A FD&C Red No. 3 ("fd and c red no 3"); B FD&C Red No. 40 ("fd and c red no 40"); B FD&C Yellow No. 6 ("fd and c yellow no 6") · Report an error - GUAVA MARMALADE, GUAVA · UPC 74566131225 · FoodData Central record of Apr 27, 2023
B FD&C Red No. 40 ("red 40") · Report an error - GUAVA MARMALADE, GUAVA · UPC 74566131317 · FoodData Central record of Jun 29, 2023
B FD&C Red No. 40 ("red 40") · Report an error
Labels change: each row shows the date of its FoodData Central record. A brand that has changed a recipe can report it with "Report an error".
FDA warning letters to Ancel Products Inc, Oct 28, 2021 to Oct 28, 2026
None found from FDA food offices.
FDA notes that later events may have changed the regulatory status of what a letter discusses.