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Lower risk Food recall · FDA · Published March 30, 2021

Motha Jelly Crystals Recall: Undeclared Dyes in Mixed Fruit Jelly

USA LANKA INC recalls Motha Jelly Crystals due to undeclared and unapproved food dyes. Consumers should check product labels for batch numbers and expiration dates.

🇺🇸 FDA recall #F-0446-2021FoodMotha ›
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Recalling firmUSA LANKA INC454 Meacham Ave · Elmont, NY 11003-3852
✎ GovInfoNow plain-language explainer

USA LANKA INC is recalling Motha Jelly Crystals because they contain undeclared and unapproved food dyes. This could pose health risks if consumed, especially for people sensitive to certain dyes. Read more at govinfonow.com/recall/14737-motha-jelly-crystals-recall-undeclared-dyes-in-mixed-fruit-jelly.

Source Summary by GovInfoNow · govinfonow.com/recall/14737-motha-jelly-crystals-recall-undeclared-dyes-in-mixed-fruit-jelly · Updated October 4, 2026 · FDA enforcement record: FDA #F-0446-2021

Cite this page

“Motha Jelly Crystals Recall: Undeclared Dyes in Mixed Fruit Jelly.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14737-motha-jelly-crystals-recall-undeclared-dyes-in-mixed-fruit-jelly. Based on FDA recall #F-0446-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0446-2021%22&limit=1).

The FDA announced on March 30, 2021, that USA LANKA INC voluntarily recalled Motha Jelly Crystals due to undeclared food dyes. The product contains FD&C yellow #5, blue #1, and unapproved carmoisine. Consumers should stop consuming the jelly immediately.

How to tell if you have it

  • Brand: Motha
  • Product: Motha Jelly Crystals - Mixed Fruit Flavoured Jelly, Net Wt. 100g
  • UPC: 4792551000405
  • Expiration Date: 08/15/2022
  • Batch Code: C0818 B

The hazard

The jelly contains undeclared FD&C yellow #5 and blue #1, as well as unapproved carmoisine (E122)/dye 14720/acid red 14. The FDA classified this recall as Class II.

Context

GovInfoNow's records show other recent recalls of similar products include Sungal Jelly Snacks Recall: Undeclared Food Dyes in Product (2026-02-12) and 52USA Popping Boba Recall: Unapproved Food Dyes in Passion Fruit Flavor (2026-04-13). Additional similar recalls include 52USA Popping Boba Mango Flavor Recall: Unapproved Food Dyes Risk (2026-04-13).

How to tell if you have this one

Check the product label for the batch number C0818 B and expiration date 08/15/2022. The UPC code is 4792551000405 for identification.

  • Brand
    Motha
  • Product
    Motha Jelly Crystals - Mixed Fruit Flavoured Jelly, Net Wt. 100g
  • Category
    Food
FDA recall event · 5 products

All 5 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Status
    Terminated
  • Distribution
    NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX
Recall numberProduct, codes & lotsQuantityClass
F-0446-2021Motha Jelly Crystals - Mixed Fruit Flavoured Jelly, Net Wt. 100g,; EXP: 08/15/2022, BATCH#: C0818 B; UPC#: 4792551000405271 unitsClass II
F-0447-2021Motha Jelly Crystals - Black Currant Flavoured Jelly, Net Wt. 100g; EXP: 02/18/2022, BATCH#: C0219 A; UPC#: 4792551000047268 unitsClass II
F-0448-2021Motha Jelly Crystals - Mango Flavoured Jelly, Net Wt. 100g; EXP: 05/22/2022, UPC#: 4792551000344, BATCH#: C0523557 unitsClass II
F-0449-2021Motha Jelly Crystals Strawberry Flavoured Jelly , Net Wt. 100g; EXP: 08/15/2022, UPC#: 4792551000016, BATCH#: C0825 B577 unitsClass III
F-0450-2021Motha Jelly Crystals - Orange Flavoured Jelly, Net Wt. 100g; EXP: 05/18/2022, UPC#: 4792551000313, BATCH#: C0519433 unitsClass II
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the batch number C0818 B and expiration date 08/15/2022 on the label.

Where it went and when

Where it was distributed

Distributed in 10 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: yesMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Connecticut, Maryland, Massachusetts, Mississippi, New Jersey, New York, North Carolina, Pennsylvania, Texas.

Recall timeline

FDA terminated this recall 14 months after the firm started it.

1. Firm started the recall: Mar 30, 202112. FDA classified it Class II: Apr 21, 202123. Published in FDA’s Enforcement Report: Apr 28, 202134. FDA terminated the recall: May 18, 2022420212022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0446-2021 (March 30, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0446-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA