RecallHawk
Class I Recall

Dr. Snack Goji Berry; PACKED FOR B.C.S. INTERNATIONAL CORP; 4.5oz, 6oz, 9oz packs clear plastic packs and 5lb cardboard

B.C.S. International Corporation

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

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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