Deskins Candies, Peanut Butter No Bake,16 oz., Plastic Shell, 12-16oz. packages per case.
Deskins Wholesale, LLC recalled this product and the FDA reported the enforcement action on 22 June 2022 as Class I. The recall was initiated by the firm. Products were made with peanut butter contaminated with Salmonella.

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
- Deskins Candies, Peanut Butter No Bake,16 oz., Plastic Shell, 12-16oz. packages per case.
- Reason for recall
- Products were made with peanut butter contaminated with Salmonella.
- Recalling firm
- Deskins Wholesale, LLC
- Firm location
- Bluefield, West Virginia, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-1311-2022
- Quantity
- 167 Cases
- Distribution
- The products were distributed domestically, WV, VA, and NC .
- Initiated
- 22 May 2022
- Reported by FDA
- 22 June 2022
- Terminated
- 19 September 2023
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Peanut Butter No-Bake 733980123314
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. 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 4 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 4 separate recalls, which almost every published figure does, overstates it by a factor of 4. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 4 of them.
- The recall ran for 16 months, from 22 May 2022 to termination on 19 September 2023. 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 2 states, and the FDA published the enforcement report 4 weeks 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: West Virginia, 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
Salmonella
Salmonella is a bacterium that survives in low-moisture foods for months, which is why it appears in recalls of products that carry no water for it to grow in: nut butters, spices, flour and dry pet food.
A preventive controls plan covers Salmonella contamination 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 117.135(c)(1)
- Process controls: the controls that apply a treatment, such as a validated kill step, at the point where it reduces the hazard to a safe level.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
- 21 CFR 117.165(a)(2)
- Product testing: testing as a verification activity, appropriate to the facility, the food and the nature of the preventive control.
Filed under milk and dairy and nuts and seeds. A product can sit in more than one.
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 Deskins Wholesale, LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2022-06-22 | Deskins Candies, Peanut Butter Pinwheel ,16 oz., Plastic Shell, 12-16oz. packages per case. | Deskins Wholesale, LLC | Products were made with peanut butter contaminated with Salmonella. | Class I |
| 2022-06-22 | Deskins Candies, Peanut Butter Fudge,16 oz., Plastic Shell, 12 - 16oz. packages per case. | Deskins Wholesale, LLC | Products were made with peanut butter contaminated with Salmonella. | Class I |
| 2022-06-22 | Deskins Candies, Chocolate No-Bake,16 oz., Plastic Shell, 12-16 oz. packages per case. | Deskins Wholesale, LLC | Products were made with peanut butter contaminated with Salmonella. | Class I |
| 2015-07-01 | Deskins Candies, Chocolate No Bakes, Net Wt. 16-oz., packaged in 1 lb. plastic containers containing 8-10 cookies / 12 containers per case. Deskins Wholesale, Bluefield, WV. | Deskins Wholesale, LLC | The recalled product contains undeclared peanut butter. | Class I |
All 5 records for Deskins Wholesale, LLC
All 2022 recalls · All FDA food recall data
21 CFR 117.135(c)(1) 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.