tru fru Strawberries + Creme Freeze-Dried Fresh, retail pouch 3.4oz UPC 85004...
FDA Recall #H-0093-2026 — Class II — September 25, 2025
Recall Summary
| Recall Number | H-0093-2026 |
| Date Initiated | September 25, 2025 |
| Classification | Class II |
| Status | Ongoing |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | Georgia Nut Co |
| Location | Skokie, IL |
Product Description
tru fru Strawberries + Creme Freeze-Dried Fresh, retail pouch 3.4oz UPC 850048358249, 6 retail units per case
Reason for Recall
potential for metal in product
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
These products were distributed in the United States. Consumers may have purchased impacted product via retail stores and online retail, including but not limited to: Albertson s, CVS, Food Lion, H-E-B, Hungryroot, Ingles Markets, Kroger, Stew Leonard s, and Target.
Product Quantity
76121 cases
Product Codes / Lot Numbers
520B15GN20 520B25GN20 520B35GN20 520C15GN20 520C25GN20 520C35GN20 520D15GN20 520D25GN20 520D35GN20 520E15GN20 520E15GN22 520E25GN20 520E25GN22 520E35GN20 520E35GN22 520F15GN20 520F15GN22 520F25GN20 520F25GN22 520F35GN20 520F35GN22 521A15GN22 524C15GN22 524C25GN22 524C35GN22 524D15GN22 524D25GN22 524D35GN22 524E15GN22 524E25GN22
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.
Foreign objects in food — including metal fragments, plastic pieces, glass shards, or rubber — can cause a range of injuries. Dental injuries (chipped or broken teeth) are the most common result. Metal and glass fragments can cause lacerations to the mouth, throat, esophagus, or intestinal tract. Hard objects may also pose a choking hazard, particularly for children and the elderly. If you consumed food containing a foreign object and are experiencing pain, difficulty swallowing, or bleeding, seek medical attention immediately. If the object was metal or glass and you swallowed it, an X-ray may be needed to determine its location.
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.