CLASS I Food recall · Reported 15 Jun 2022 · FDA Enforcement Report
Garden Highway, Protein Power Snack . in a, Keep Refrigerated recalled
F&S Produce is recalling Garden Highway, Protein Power Snack . in a, Keep Refrigerated. The recall was initiated on 23 May 2022 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1282-2022
- FDA event ID
- 90276
- Recalling firm
- F&S Produce, Vineland, NJ
- Brand
- Garden Highway
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 23 May 2022
- FDA classified
- 9 Jun 2022
- Reported
- 15 Jun 2022
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Salmonella
- Product category
- Other
Timeline
| 23 May 2022 | Recall initiated by company | |
| 9 Jun 2022 | Classified by FDA | +17 days |
| 15 Jun 2022 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product was made with peanut butter contaminated with Salmonella.
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
Garden Highway, Protein Power Snack, 7.25 oz . in a Plastic Container, Keep Refrigerated .
Where it was distributed
The product was distributed domestically.
Questions about this recall
Why was it recalled?
Product was made with peanut butter contaminated with Salmonella.
Which lots are affected?
Best By: 05/24/22, 05/26/22, 05/28/22
Where was it sold?
The product was distributed domestically.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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