PROSANTE TVGPTN 10B MNCD 25LB BG/40P, PROSANTE TVGPTN 10B MNCD 800LB TT, PROS...
FDA Recall #F-0785-2023 — Class II — March 30, 2023
Recall Summary
| Recall Number | F-0785-2023 |
| Date Initiated | March 30, 2023 |
| Classification | Class II |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | Cargill, Inc Corporate Headquarters |
| Location | Wayzata, MN |
Product Description
PROSANTE TVGPTN 10B MNCD 25LB BG/40P, PROSANTE TVGPTN 10B MNCD 800LB TT, PROSANTE TVGPTN 10B MNCD 50LB BG, PROSANTE TVGPTN 10B MNCD 50LB BG 21/P; distributed in bulk tote and paper bags
Reason for Recall
Products with a gluten free claim may contain gluten levels above 20 ppm.
Classification
Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution Pattern
Nationwide United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and United Kingdom
Product Quantity
4,636,250 lbs
Product Codes / Lot Numbers
100001356-00223CHXEA 100001356-00323CHXEA 100001356-01023CHXEA 100001356-01123CHXEA 100001356-01223CHXEA 100001356-01323CHXEA 100001356-03223CHXEA 100001356-04523CHXEA 100001356-04623CHXEA 100001356-04723CHXEA 100001356-05823CHXEA 100001356-28422CHXEA 100001356-28522CHXEA 100001356-28622CHXEA 100001356-30722CHXEA 100001356-31822CHXEA 100001356-31922CHXEA 100001356-33422CHXEA 100001356-33522CHXEA 100001356-33622CHXEA 100001356-34922CHXEA 100001361-01123CHXTA 100001361-01223CHXTA 100001361-04423CHXTA 100001364-00323CHXEA 100001364-00423CHXEA 100001364-00523CHXEA 100001364-00623CHXEA 100001364-02523CHXEA 100001364-02623CHXEA 100001364-03323CHXEA 100001364-27822CHXEA 100001364-27922CHXEA 100001364-28122CHXEA 100001364-29822CHXEA 100001364-29922CHXEA 100001364-30022CHXEA 100001364-30122CHXEA 100001364-30822CHXEA 100001364-32222CHXEA 100001364-32422CHXEA 100001364-32522CHXEA 100001364-32622CHXEA 100001364-32722CHXEA 100001364-35522CHXEA 100001364-35622CHXEA 100001364-36122CHXEA 100001364-36222CHXEA 100001364-36322CHXEA 130012781-00323CHXEA 130012781-03223CHXEA 130012781-05123CHXEA 130012781-29722CHXEA 130012781-29822CHXEA 130012781-32522CHXEA
What Should You Do?
Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.
Frequently Asked Questions
Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.
In most cases, yes. Retailers are typically notified to accept returns of recalled products and issue refunds, regardless of whether you have a receipt. Check with the store where you purchased the item. Some manufacturers also offer direct refunds — contact the recalling firm using the information in the official recall notice. If you purchased the product online, contact the retailer's customer service with your order number. In either case, you generally do not need original packaging, though retaining the product label with the lot code or UPC can speed up the process.
Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.
The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.