Class IF-0674-2024

Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.

Product

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

Type: Food
Affected lot / code info: Use By Start Dates: 11/7/2023, 23300, 11/2/2023, 23296, 11/3/2023, 11/14/2023 Use by End Dates:11/7/2023, 23314, 11/23/2023, 11/21/2023, 23317, 11/24/2023, 11/21/2023
Quantity: 3202 units

Why it was recalled

Potential Salmonella Contamination

Recalling firm

Firm: TGD Cuts, LLC
Notification channel: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Type: Voluntary: Firm initiated
Address: 8441 Dorsey Run Rd Unit B, N/A, Jessup, Maryland 20794-9359

Distribution

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

Timeline

Recall initiated: 2023-11-29
FDA classified: 2024-01-02
Posted by FDA: 2023-12-27
Terminated: 2024-09-25
Status: Terminated

Source: openFDA Food Enforcement endpoint. Recall record F-0674-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings.