Dr. Snack Goji Berry; PACKED FOR B.C.S. INTERNATIONAL CORP; 4.5oz, 6oz, 9oz packs clear plastic packs and 5lb cardboard
Summary
The FDA issued a Class I for Dr. Snack Goji Berry; PACKED FOR B.C.S. INTERNATIONAL CORP; 4.5oz, 6oz, 9oz pack by B.C.S. International Corporation. Reason: Product contains undeclared sulfites..
Details
Source
Food Recall
External ID
F-0720-2022
Action Date
2022-02-16
Status
Terminated
Category
food
Product Description
Dr. Snack Goji Berry; PACKED FOR B.C.S. INTERNATIONAL CORP; 4.5oz, 6oz, 9oz packs clear plastic packs and 5lb cardboard boxes
Lot/Code Info: UPC: 80555492205, 80555493218, 80555494216 or 80555470198.
Quantity Affected: 937pcs
Reason for Recall
Product contains undeclared sulfites.
Distribution
NY, NJ, PA,RI
Type: Voluntary: Firm initiated
Recall Initiated: 2022-01-19
Company
Long Island City, NY
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 115 food recalls issued in the same week, part of 204 food-related FDA actions this month.
B.C.S. International Corporation has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (B.C.S. International Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does B.C.S. International Corporation have FDA actions?
B.C.S. International Corporation has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0720-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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