Class IITerminated in FDA datasetRecall initiated Aug 15, 2018

Sammy Salsa Roasted Cabo Verde, packaged in 14 oz. plastic container, 6 units per case.

Recalling firm: Sammy Food Products LLC

Why it was recalled

Salsa products are recalled due to a potential contamination with Cyclospora. Salsa products contain cilantro that was recalled due to a potential contamination with Cyclospora.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 19, 2018.

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Compare the exact product and package details with the label you have.

ProductSammy Salsa Roasted Cabo Verde, packaged in 14 oz. plastic container, 6 units per case. UPC # 00868422000141. The label is read in parts: "***Roasted Tomatillos, Roasted Onion, Roasted Chile Peppers, Roasted Garlic, Fresh Cilantro, Fresh Lime, Water, Organic Vegetable Stock (water, Carrots, Onion, Celery, Tomatoes, Leeks, Sea Salt, Mushrooms, Garlic, Savory Leaf, Ground Bay Leaf), Granulated Garlic, Sea Salt, Pepper, Spices. Contains less than 2% of Vinegar, Calcium Acetate ***".
Package size14 oz

FDA code information

Use by date of Sept 9/18

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Full FDA record and distribution details

Original product description

Sammy Salsa Roasted Cabo Verde, packaged in 14 oz. plastic container, 6 units per case. UPC # 00868422000141. The label is read in parts: "***Roasted Tomatillos, Roasted Onion, Roasted Chile Peppers, Roasted Garlic, Fresh Cilantro, Fresh Lime, Water, Organic Vegetable Stock (water, Carrots, Onion, Celery, Tomatoes, Leeks, Sea Salt, Mushrooms, Garlic, Savory Leaf, Ground Bay Leaf), Granulated Garlic, Sea Salt, Pepper, Spices. Contains less than 2% of Vinegar, Calcium Acetate ***".

Original FDA recall reason

Salsa products are recalled due to a potential contamination with Cyclospora. Salsa products contain cilantro that was recalled due to a potential contamination with Cyclospora.

Recall details

Recall number
F-1952-2018
Event ID
80897
FDA status
Terminated
Initiated
Aug 15, 2018
Reported
Sep 12, 2018
Classified
Sep 4, 2018
Terminated
Sep 19, 2018
Quantity
10 cases
Location
Portland, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

distributed in Oregon and Washington

FDA source record · F-1952-2018

Data updated September 16, 2026. View official FDA data ↗

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