FDA recall record

TGD Cuts Cantaloupe Chunks/Spears: Cantaloupe Chunks 1" 50/2 oz recall — FDA F-0674-2024

Potential Salmonella Contamination

Class Iclassification
F-0674-2024official record ID
Dec 27, 2023report date

Recall record at a glance

Official recordF-0674-2024
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmTGD Cuts, LLC
Report dateDec 27, 2023
Recall initiation dateNov 29, 2023
Quantity3202 units
LocationJessup, MD, United States

Official product description

Cantaloupe Chunks/Spears: Cantaloupe Chunks 1" 50/2 oz. Packaged in film UPC: 840219184845 Cantaloupe Chunks 1" 2/5 lb. Packaged in trays. UPC: 840219184449 Cantaloupe Chunks 6/16oz. Packaged in clamshell containers. UPC: 840219150345 Cantaloupe Chunks 50/2 oz. Packaged in film. UPC: 840219186030 Cantaloupe Chunks 4/2.5 lb. Packaged in trays. UPC: 840219185231 Cantaloupe Chunks 20 lb. Packaged in buckets. UPC: 840219170190 Cantaloupe Chunks 3/30 oz. Packaged in clamshell containers. UPC: 840219150338 Cantaloupe Chunks 5 lb. Packaged in trays. UPC: 840219134499 Cantaloupe Chunks 2/5 lb. Packaged in trays. UPC: 840219196701 Cantaloupe Chunks 4/6 oz. Packaged in clamshell containers. UPC: 840219198569 Cantaloupe Chunks 6/9 oz. Packaged in clamshell containers. UPC: 840219165196 Cantaloupe Spears 6/16 oz. Packaged in clamshell containers. UPC: 840219163697 Cantaloupe Spears 100/2 oz. Packaged in film. UPC:840219172088 Cantaloupe Spears 50/2 oz. Packaged in film UPC:840219179452 Cantaloupe Spears 50/4 oz. Packaged in film. UPC: 840219138756

Why the product was recalled

Potential Salmonella Contamination

Distribution information

Distributed in PA, NJ, MD, WV, SC VA, DE, NC, and NY

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.