Watson Pickled Garlic Ail Marine; 500g (18 oz. plastic pouch. Refrigerate after opening. UPC 8 00794 00303 0
Summary
The FDA issued a Class II for Watson Pickled Garlic Ail Marine; 500g (18 oz. plastic pouch. Refrigerate after by WATSON LA INC. Reason: 40 cases of product that had been detained by FDA for high lead levels were distributed..
Details
Source
Food Recall
External ID
F-0773-2021
Action Date
2021-07-21
Status
Terminated
Category
food
Product Description
Watson Pickled Garlic Ail Marine; 500g (18 oz. plastic pouch. Refrigerate after opening. UPC 8 00794 00303 0
Lot/Code Info: No codes. Shipping dates of April 14-27, 2021.
Quantity Affected: 40 cases (24 x 500 g pouches per case)
Reason for Recall
40 cases of product that had been detained by FDA for high lead levels were distributed.
Distribution
WA, CA
Type: Voluntary: Firm initiated
Recall Initiated: 2021-05-03
Company
Diamond Bar, 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 17 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 (WATSON LA INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does WATSON LA INC have FDA actions?
This is the only FDA action we have on record for WATSON LA INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0773-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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