FDA Recall United States Terminated Historical recordClass II
Michael Zakany LLC
- Product
- Jose Madrid Salsa Chipotle Con Queso, Net Wt. 13 oz. (369g),…
- Published
- December 11, 2024
- Distribution
- Product was sold through 6 distributors…
Michael Zakany LLC Recall: Undeclared anchovy allergen
United States
TerminatedClass II
- Company
- Michael Zakany LLC
- Product
- Jose Madrid Salsa - Strawberry Mild Salsa 13oz glass jars,…
- Recall date
- April 14, 2021
- Terminated
- June 2, 2021
- Source
- FDA
Reason for recall
Undeclared anchovy allergen
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Jose Madrid Salsa - Strawberry Mild Salsa 13oz glass jars, 12 jars per case | Not published in this source record | 6,659 jars | Facility Code 601 Product Code 19 Batch Code 01 Serial Number 6011901 032924 Best By Date 03/26/20 - 03/29/24 |
Distribution
- Product is sold at local farmer's markets
- 12 retail locations within Ohio
- 1 distributor in Ohio
- and online sales across the US. Estimate on sales: 1
- 099 jars sold through websites
- 800 sold through local fundraisers
- 400 sold at retailers
- 200 through distributor
- 1
- 000 for samples at events
- 60 jars held for retain samples/testing
- 2
- 500 sold at craft fairs/farmer's markets.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0473-2021
- Event ID
- 87726
- Status
- Terminated
- Classification
- Class II
- Company
- Michael Zakany LLC
- Product description
- Jose Madrid Salsa - Strawberry Mild Salsa 13oz glass jars, 12 jars per case
- Quantity
- 6,659 jars
- Reason
- Undeclared anchovy allergen
- Recall initiation date
- April 14, 2021
- Report date
- May 5, 2021
- Classification date
- Not published in this source record
- Termination date
- June 2, 2021
- Distribution pattern
- Product is sold at local farmer's markets, 12 retail locations within Ohio, 1 distributor in Ohio, and online sales across the US. Estimate on sales: 1,099 jars sold through websites, 800 sold through local fundraisers, 400 sold at retailers, 200 through distributor, 1,000 for samples at events, 60 jars held for retain samples/testing, 2,500 sold at craft fairs/farmer's markets.
- UPC, lot, and code information
- Facility Code 601 Product Code 19 Batch Code 01 Serial Number 6011901 032924 Best By Date 03/26/20 - 03/29/24
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Michael Zakany LLC
Other recalls from Michael Zakany LLC
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 II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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.
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