Hartley's brand Worcestershire sauce in 1 gallon plastic bottles and 50 gallon drums.
Summary
The FDA issued a Class I for Hartley's brand Worcestershire sauce in 1 gallon plastic bottles and 50 gallon d by H & H Products Company. Reason: Undeclared allergen: FISH (anchovies) on product labeling..
Details
Source
Food Recall
External ID
F-0762-2021
Action Date
2021-07-07
Status
Terminated
Category
food
Product Description
Hartley's brand Worcestershire sauce in 1 gallon plastic bottles and 50 gallon drums.
Lot/Code Info: Lot numbers: HH21-138; HH20-349; HH21-053; HH21-113; HH21-067; HH21-131; HH210-113
Quantity Affected: 1 gallon bottles: 3,184; 50 gallon drums: 16
Reason for Recall
Undeclared allergen: FISH (anchovies) on product labeling.
Distribution
Product was sold to distributors in FL, AL, GA in 1 gallon and 50 gallon drums.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-06-23
Company
Orlando, FL
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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (H & H Products Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does H & H Products Company have FDA actions?
This is the only FDA action we have on record for H & H Products Company in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0762-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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