CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS, ROSEMONT, I...
FDA Recall #H-0502-2026 — Class II — April 30, 2025
Recall Summary
| Recall Number | H-0502-2026 |
| Date Initiated | April 30, 2025 |
| Classification | Class II |
| Status | Ongoing |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | Ventura Foods LLC |
| Location | Los Angeles, CA |
Product Description
CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS, ROSEMONT, IL 60018; PEANUT BUTTER NET WT. 0.5OZ & NET WT 0.75OZ DIST BY: DYMA BRANDS, INC. ATLANTA, GA 30328; Product also sold under the following brand names: FLAVOR Fresh PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY: DYMA BRANDS, INC. ATLANTA, GA 30328; HOUSE RECIPE CREAMY PEANUT BUTTER NET WT 0.75 OZ (21.2g) DISTRIBUTED BY SYSCO COROPRATION, HOUSTON, TEXAS 77077; Katy's Kitchen SMOOTH PEANUT BUTTER NET WT 0.75 OZ (21g) MARKETED BY INDEPENDENT MARKETING ALLIANCE HOUSTIN, TX 77043 PEANUT BUTTER creamy NET WT 0.75 OZ (21g) FOR DISTRIBUTION EXCLUSIVELY BY GORDON FOOD SERVICE WYOMING, MI 49509; CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328
Reason for Recall
Foreign material. During production, the firm found pieces of blue plastic in a filter.
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
Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA & WI.
Product Quantity
17,115cs/.75oz pkgs + 4,496cs/.5oz pkgs + 516cs/1.12oz pkgs
Product Codes / Lot Numbers
88652: Lot# D077F01, Lot# D079F01, Lot# D080F01, Lot# D083F01, Lot# D084F01, Lot# D086F01, Lot# D087F01, Lot# D090F01, Lot# D091F01, Lot# D092F01, Lot# D093F01, Lot# D095F01, Lot# D097F01, Lot# D098F01, Lot# D099F01, Lot# D106F01, Lot# D107F01 88640: Lot# D076F01, Lot# D085F01, Lot# D102F01 72445: Lot# D077F01, Lot# D078F01, Lot# D079F01, Lot# D085F01, Lot# D091F01, Lot# D092F01, Lot# D100F01, Lot# D101F01, Lot# D102F01, Lot# D104F01 & Lot# D105F01. 88660: Lot# D077F01, Lot# D076F01, Lot# D102F01 96435: Lot# D080F01, Lot# D094F01 86442: Lot# D100F02, Lot# D101F02 86433: Lot# D077F02, Lot# D078F02, Lot# D083F02, Lot# D084F02, Lot# D086F02, Lot# D104F02, Lot# D105F02, Lot# D106F02, Lot# D107F02
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.