CLASS I Food recall · Reported 13 Aug 2025 · FDA Enforcement Report
Parashore Pear Slices in Juice recalled by W.W. Industrial Group
W.W. Industrial Group is recalling Parashore Pear Slices in Juice, distributed in California. The recall was initiated on 21 Jul 2025 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-0387-2025
- FDA event ID
- 97310
- Recalling firm
- W.W. Industrial Group, New Hyde Park, NY
- Brand
- Parashore Pear
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 21 Jul 2025
- FDA classified
- 4 Aug 2025
- Reported
- 13 Aug 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Lead & Heavy Metals
- Product category
- Juice
Timeline
| 21 Jul 2025 | Recall initiated by company | |
| 4 Aug 2025 | Classified by FDA | +14 days |
| 13 Aug 2025 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Contaminated with elevated lead and cadmium
Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.
Product as listed by the FDA
Parashore Pear Slices in Juice, 15 oz. (425 g), UPC#704817164237
Where it was distributed
CA
Questions about this recall
Why was it recalled?
Contaminated with elevated lead and cadmium
Which lots are affected?
Lot 3700/01172 6122J Prod: 02/19/2024, Best by 2/19/2027
Where was it sold?
CA
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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