CLASS I ONGOING Food recall · Reported 3 Jun 2026 · FDA Enforcement Report
(Bulk) Spl-bev Banana Cwt (Banana Smoothie) recalled by Honeyville
Honeyville is recalling (Bulk) Spl-bev Banana Cwt (Banana Smoothie), distributed in California, Utah. The recall was initiated on 21 Apr 2026 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
- H-0849-2026
- FDA event ID
- 98841
- Recalling firm
- Honeyville, Ogden, UT
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 21 Apr 2026
- FDA classified
- 22 May 2026
- Reported
- 3 Jun 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Salmonella
- Product category
- Juice
Timeline
| 21 Apr 2026 | Recall initiated by company | |
| 22 May 2026 | Classified by FDA | +31 days |
| 3 Jun 2026 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.
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
(BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099
Where it was distributed
Distribution is to California and Utah consignees.
Questions about this recall
Why was it recalled?
Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.
Which lots are affected?
Lot number# 0325357B201
Where was it sold?
Distribution is to California and Utah consignees.
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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