Tea Wafer - Vanilla Almond [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]
Summary
The FDA issued a Class II for Tea Wafer - Vanilla Almond [Two sizes: retail package of 8 wafers (7 oz) and ret by Sacramento Cookie Factory. Reason: Undeclared allergen (milk).
Details
Source
Food Recall
External ID
F-1216-2024
Action Date
2024-05-15
Status
Ongoing
Category
food
Product Description
Tea Wafer - Vanilla Almond [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]
Lot/Code Info: All best by dates up to 4/2/2025 (shelf life is 1 year from manufacture date). Firm does not apply lot codes.
Quantity Affected: Retail package of 8 wafers: 464 units; Retail Gift of 2 wafers: 162 units
Reason for Recall
Undeclared allergen (milk)
Distribution
U.S. Distribution to the following states: CA, AK, IA, NY, TX, FL, WA, NJ, WA, VA, GA, TN, AZ, AL, NC. For foreign or government distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-04-17
Company
Sacramento, CA
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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Sacramento Cookie Factory has 5 FDA actions in our database, including 5 recalls.
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 (Sacramento Cookie Factory) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Sacramento Cookie Factory have FDA actions?
Sacramento Cookie Factory has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1216-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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