CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS, ROSEMONT, IL 60018…
Ventura Foods LLC recalled this product and the FDA reported the enforcement action on 18 February 2026 as Class II. The recall was initiated by the firm. Foreign material. During production, the firm found pieces of blue plastic in a filter.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- 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.
- Recalling firm
- Ventura Foods LLC
- Firm location
- Los Angeles, California, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- H-0502-2026
- Quantity
- 17,115cs/.75oz pkgs + 4,496cs/.5oz pkgs + 516cs/1.12oz pkgs
- Distribution
- 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.
- Initiated
- 30 April 2025
- Reported by FDA
- 18 February 2026
- Terminated
- 23 March 2026
- Firm notified by
- Letter
- Product codes
- 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
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 3 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 3 separate recalls, which almost every published figure does, overstates it by a factor of 3. All 3 of them are listed on this page.
- The recall ran for 11 months, from 30 April 2025 to termination on 23 March 2026. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 37 states, and the FDA published the enforcement report 10 months after the firm began the recall.
- Recalls of milk or a dairy product run a median of 7 months, so this one was longer than usual for its category. Dairy recalls split between pathogen contamination in products that skipped or under-ran pasteurisation and undeclared milk in products that should never have contained it, which is the same allergen viewed from two directions.
Named in the distribution pattern: Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Foreign material
A foreign material recall means something that is not food was found in food: metal, plastic, glass, wood or insect matter, usually shed by equipment during processing.
A preventive controls plan covers foreign material under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.40
- Equipment and utensils: plant equipment designed and maintained so it cannot contaminate food with lubricants, fuel, metal fragments or contaminated water.
- 21 CFR 117.80(c)
- Manufacturing operations: the measures that protect food from contamination during processing, including the effective ones against metal and other extraneous material.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Filed under milk and dairy and nuts and seeds. A product can sit in more than one.
Every product in this recall
The FDA opened 3 enforcement records for this one recall, one per product code. This page carries all of them; the 2 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2026-02-18 | CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/STRAWBERRY JAM NET WT 1 OZ (28g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328 CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/STRAWBERRY JAM NET WT 1 OZ (28g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328 | Ventura Foods LLC | Foreign material. During production, the firm found pieces of blue plastic in a filter. | Class II |
| 2026-02-18 | CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/GRAPE JELLY NET WT 1 OZ (28g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328 CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/GRAPE JELLY NET WT 1 OZ (28g) POCO PAC DISTRIBUTED BY DYMA BRANDS, INC. ATLANTA, GA 30328 | Ventura Foods LLC | Foreign material. During production, the firm found pieces of blue plastic in a filter. | Class II |
Other milk and dairy recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Ventura Foods LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 25 other records name this firm.
All 26 records for Ventura Foods, LLC
All 2026 recalls · All FDA food recall data
21 CFR 117.40 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.