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W.W. Industrial Group, Inc. Recall: Contaminated with elevated lead and cadmium

United States

TerminatedClass I

Company
W.W. Industrial Group, Inc.
Product
Parashore Pear Slices in Juice, 15 oz. (425 g), UPC#70481716…
Recall date
July 21, 2025
Terminated
November 5, 2025
Source
FDA

Reason for recall

Contaminated with elevated lead and cadmium

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Parashore Pear Slices in Juice, 15 oz. (425 g), UPC#704817164237 Not published in this source record 8160 units Lot 3700/01172 6122J Prod: 02/19/2024, Best by 2/19/2027

Distribution

  • CA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0387-2025
Event ID
97310
Status
Terminated
Classification
Class I
Company
W.W. Industrial Group, Inc.
Product description
Parashore Pear Slices in Juice, 15 oz. (425 g), UPC#704817164237
Quantity
8160 units
Reason
Contaminated with elevated lead and cadmium
Recall initiation date
July 21, 2025
Report date
August 13, 2025
Classification date
Not published in this source record
Termination date
November 5, 2025
Distribution pattern
CA
UPC, lot, and code information
Lot 3700/01172 6122J Prod: 02/19/2024, Best by 2/19/2027
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: W.W. Industrial Group, Inc.

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
California 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.