← FDA ENFORCEMENT
F-0674-2024Class I

TGD Cuts, LLC

Recalling firm
TGD Cuts, LLC
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2023-12-27
Distribution
Distributed in PA, NJ, MD, WV, SC VA, DE, NC, and NY
Firm state
MD
Product quantity
3202 units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Potential Salmonella Contamination

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

Code / lot 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

Other recalls SPEQ maps to Environmental Monitoring
2026-07-22Class IArgon Medical Devices, Inc2026-07-22Class IIOlympus Corporation of the Americas2026-07-22Class IIChiesi USA, Inc.2026-07-22Class IICareFusion 213, LLC
See all Environmental Monitoring recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.