FDA recall record

Baroody Imports Beirut Lift Turnip Pickles Imported & Distributed By: Baroody recall — FDA F-0323-2017

Beirut Lift Turnip Pickles contain undeclared beet root red color.

Class IIclassification
F-0323-2017official record ID
Nov 16, 2016report date

Recall record at a glance

Official recordF-0323-2017
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBaroody Imports Inc.
Report dateNov 16, 2016
Recall initiation dateJan 4, 2016
Quantity700 g - 5,580 containers; 2 kg - 1200 containers; 10 kg- 50 pails
LocationClifton, NJ, United States

Official product description

Beirut Lift Turnip Pickles Imported & Distributed By: Baroody Import Inc. 1500 B Main Ave. -Clifton, NJ 07011 Tel: 973.3404832 700 g - UPC 642036014141 2 kg - UPC 642036014219 10 kg - UPC

Why the product was recalled

Beirut Lift Turnip Pickles contain undeclared beet root red color.

Distribution information

CT, NJ & NY

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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.