Monfefo brand Turmeric Shot; 2oz; Cold Pressed Juice Blend; packaged in glass bottle
Summary
The FDA issued a Class II for Monfefo brand Turmeric Shot; 2oz; Cold Pressed Juice Blend; packaged in glass bo by Monfefo LLC. Reason: Product was not manufactured according to specifications..
Details
Source
Food Recall
External ID
F-0860-2021
Action Date
2021-08-18
Status
Terminated
Category
food
Product Description
Monfefo brand Turmeric Shot; 2oz; Cold Pressed Juice Blend; packaged in glass bottle
Lot/Code Info: Turmeric Shot 12 pack: UPC 660002515441 Turmeric Shot single shot: UPC 860002515410 LOTS: 1942128; 1882127; 1792126 EXP: 8/17/21; 8/23/21; 9/14/21; 9/21/21
Quantity Affected: 25 cases
Reason for Recall
Product was not manufactured according to specifications.
Distribution
NY, NJ, CT, TX, MD, DC, FL, ME, MA, VT, OH, PA, VA, GA, NC, SC, WI, CO, CA
Type: Voluntary: Firm initiated
Recall Initiated: 2021-07-26
Company
Brooklyn, NY
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Monfefo LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Monfefo LLC have FDA actions?
This is the only FDA action we have on record for Monfefo LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0860-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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