Seasoned Garlic with Salt and Vinegar distributed in un-labeled plastic containers 6oz…
Lemonland Food Corp recalled this product and the FDA reported the enforcement action on 5 April 2023 as Class III. The recall was initiated by the firm. Seasoned Garlic with Salt and Vinegar was removed because the firm provided the updated ingredients statement to consignees. Product does not contain any allergens.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Seasoned Garlic with Salt and Vinegar distributed in un-labeled plastic containers 6oz, 8oz, and 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
- Reason for recall
- Seasoned Garlic with Salt and Vinegar was removed because the firm provided the updated ingredients statement to consignees. Product does not contain any allergens.
- Recalling firm
- Lemonland Food Corp
- Firm location
- Kent, Washington, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- F-0666-2023
- Quantity
- 6oz containers = 2.53 lb; 8oz containers = 28.77 lb; 12oz. containers = 56.20 lb.
- Distribution
- Distributed in Washington
- Initiated
- 23 February 2023
- Reported by FDA
- 5 April 2023
- Terminated
- 29 March 2023
- Firm notified by
- Product codes
- Feb. 16, 2023 to Feb. 23, 2023.
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 31 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 31 separate recalls, which almost every published figure does, overstates it by a factor of 31. All 31 of them are listed on this page.
- The recall ran for 5 weeks, from 23 February 2023 to termination on 29 March 2023. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The FDA published the enforcement report 6 weeks after the firm began the recall.
- Recalls of a spice or seasoning run a median of 6 months, so this one was shorter than usual for its category. Spices are a low-moisture, globally sourced, minimally processed ingredient that is added after any kill step, which is the combination that makes Salmonella in a spice lot capable of contaminating every product it was blended into.
Filed under spices and seasonings. A product can sit in more than one.
Every product in this recall
The FDA opened 31 enforcement records for this one recall, one per product code. This page carries all of them; the 30 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
Other spices and seasonings recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Lemonland Food Corp
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 43 other records name this firm.
All 44 records for Lemonland Food Corp
All 2023 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.