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USA LANKA INC Recall: Jelly contain undeclared FD&C yellow #5 and blue #1, and unapproved carmoisine (E122)/dye 14720/acid red 14 - F-0447-2021

United States

TerminatedClass II

Company
USA LANKA INC
Product
Motha Jelly Crystals - Black Currant Flavoured Jelly, Net Wt…
Recall date
March 30, 2021
Terminated
May 18, 2022
Source
FDA

Reason for recall

Jelly contain undeclared FD&C yellow #5 and blue #1, and unapproved carmoisine (E122)/dye 14720/acid red 14

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Motha Jelly Crystals - Black Currant Flavoured Jelly, Net Wt. 100g Not published in this source record 268 units EXP: 02/18/2022, BATCH#: C0219 A; UPC#: 4792551000047

Distribution

  • NY
  • MA
  • MD
  • CT
  • CA
  • PA
  • MS
  • NC
  • NJ
  • TX

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0447-2021
Event ID
87610
Status
Terminated
Classification
Class II
Company
USA LANKA INC
Product description
Motha Jelly Crystals - Black Currant Flavoured Jelly, Net Wt. 100g
Quantity
268 units
Reason
Jelly contain undeclared FD&C yellow #5 and blue #1, and unapproved carmoisine (E122)/dye 14720/acid red 14
Recall initiation date
March 30, 2021
Report date
April 28, 2021
Classification date
Not published in this source record
Termination date
May 18, 2022
Distribution pattern
NY, MA, MD, CT, CA, PA, MS, NC, NJ, TX
UPC, lot, and code information
EXP: 02/18/2022, BATCH#: C0219 A; UPC#: 4792551000047
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 87610 with 4 other product entries in Public Health Trace.

FDA Recall United States TerminatedTerminated: May 18, 2022Historical recordClass II

USA LANKA INC

Product
Motha Jelly Crystals - Orange Flavoured Jelly, Net Wt. 100g
Published
April 28, 2021
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: May 18, 2022Historical recordClass III

USA LANKA INC

Product
Motha Jelly Crystals Strawberry Flavoured Jelly , Net Wt. 10…
Published
April 28, 2021
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: May 18, 2022Historical recordClass II

USA LANKA INC

Product
Motha Jelly Crystals - Mango Flavoured Jelly, Net Wt. 100g
Published
April 28, 2021
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: May 18, 2022Historical recordClass II

USA LANKA INC

Product
Motha Jelly Crystals - Mixed Fruit Flavoured Jelly, Net Wt.…
Published
April 28, 2021
Distribution
Multiple states

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Responsible company: USA LANKA INC

Other recalls from USA LANKA INC

FDA Recall United States TerminatedTerminated: May 18, 2022Historical recordClass II

USA LANKA INC

Product
Motha Jelly Crystals - Orange Flavoured Jelly, Net Wt. 100g
Published
April 28, 2021
Distribution
Multiple states

View recall →

FDA Recall United States TerminatedTerminated: May 18, 2022Historical recordClass III

USA LANKA INC

Product
Motha Jelly Crystals Strawberry Flavoured Jelly , Net Wt. 10…
Published
April 28, 2021
Distribution
Multiple states

View recall →

FDA Recall United States TerminatedTerminated: May 18, 2022Historical recordClass II

USA LANKA INC

Product
Motha Jelly Crystals - Mango Flavoured Jelly, Net Wt. 100g
Published
April 28, 2021
Distribution
Multiple states

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
New York 1
Massachusetts 1
Maryland 1
Connecticut 1
California 1
Pennsylvania 1
Mississippi 1
North Carolina 1
New Jersey 1
Texas 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of May 18, 2022.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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