Whole Foods Pomegranate Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers. Product i
Summary
The FDA issued a Class I for Whole Foods Pomegranate Guacamole Dip, Keep Refrigerated. Packed in various siz by WFM Purchasing, LP. Reason: Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella..
Details
Source
Food Recall
External ID
H-1250-2026
Action Date
2026-08-26
Status
Ongoing
Category
food
Product Description
Whole Foods Pomegranate Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is applied. Products contain the following PLU Cods located under label bar code: 27908100000, 27908500000. Packed for Whole Foods Market, located at either 1745 W. Market Street, Akron, OH 44313 or 4301 W. William Cannon, Austin, TX 78749.
Lot/Code Info: Best Before/By Date: 8/7/2026 - 8/12/2026
Quantity Affected: 12,995 units total
Reason for Recall
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Distribution
AR, IA, IL, IN, KY, LA, MI, MN, MO, OH, OK, TX, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2026-08-07
Company
Austin, TX
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 53 food recalls issued in the same week, part of 82 food-related FDA actions this month.
WFM Purchasing, LP has 15 FDA actions in our database, including 15 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (WFM Purchasing, LP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does WFM Purchasing, LP have FDA actions?
WFM Purchasing, LP has 15 FDA actions in our database, including 15 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1250-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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