FDA recall record

Lydia Pack 3 Al Amir Fresh Foods Baba Ghannooj Grilled Eggplant, packaged recall — FDA F-0869-2024

Hummus product label declares Tahini but does not declare sesame.

Class Iclassification
F-0869-2024official record ID
Feb 21, 2024report date

Recall record at a glance

Official recordF-0869-2024
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmLydia Pack 3 Inc.
Report dateFeb 21, 2024
Recall initiation dateJan 19, 2024
Quantity3,000 to 4,000 packages
LocationMilwaukie, OR, United States

Official product description

Al Amir Fresh Foods Baba Ghannooj Grilled Eggplant, packaged in round plastic clear container, net wt. 8oz. There are 12 containers per case. UPC on 8oz container: 7 55134 12342 1. The recalled product label declares: Ingredients: Fresh Grilled Eggplant, Tahini Paste, Garlico (Fresh Garlic/Oil/Lemon/Salt), Garbanzo Beans, Natural Citric Acid, Salt.

Why the product was recalled

Hummus product label declares Tahini but does not declare sesame.

Distribution information

Distributed in OR and WA.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.