CLASS II Food recall · Reported 7 Oct 2020 · FDA Enforcement Report
Wild Mushroom Barley soup recalled by Hale And Hearty Soups
Hale And Hearty Soups is recalling Wild Mushroom Barley soup, distributed in 7 states. The recall was initiated on 23 Sep 2020 and the FDA has classified it as Class II.
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-0032-2021
- FDA event ID
- 86488
- Recalling firm
- Hale And Hearty Soups, Brooklyn, NY
- Brand
- Wild
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 23 Sep 2020
- FDA classified
- 20 Oct 2020
- Reported
- 7 Oct 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Soup
Timeline
| 23 Sep 2020 | Recall initiated by company | |
| 7 Oct 2020 | Published in enforcement report | +14 days |
| 20 Oct 2020 | Classified by FDA | +13 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product may contain pieces of maggots.
Product as listed by the FDA
WILD MUSHROOM BARLEY soup; Manufactured By: Hale & Hearty Soups; 2x9.6lbs; 13.8 net weight; Keep Refrigerated
Where it was distributed
NY, NJ, OH, PA, CT, MA, MD
ConnecticutMassachusettsMarylandNew JerseyNew YorkOhioPennsylvania
Questions about this recall
Why was it recalled?
Product may contain pieces of maggots.
Which lots are affected?
Expires 10/05/20 Item 466 UPC: 1 80644 00014
Where was it sold?
NY, NJ, OH, PA, CT, MA, MD
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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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|---|---|---|---|---|---|
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