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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
Recalled products
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
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
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.
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or product is unsafe beyond what the official source has published.
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