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Severino Home Made, Artisanal Small Batch Pasta, Raviolini Cheese, 9 units ...

FDA Recall #F-1823-2018 — Class III — July 25, 2018

Recall Summary

Recall NumberF-1823-2018
Date InitiatedJuly 25, 2018
ClassificationClass III
StatusTerminated
TypeVoluntary: Firm initiated
Product TypeFood

Recalling Firm

FirmSeverino Pasta Manufacturing, Inc.
LocationWestmont, NJ

Product Description

Severino Home Made, Artisanal Small Batch Pasta, Raviolini Cheese, 9 units x 9 oz per case. Expiration March 2019.

Reason for Recall

Severino Pasta Manufacturing, Inc. has initiated a recall of their Severino Pasta Super Fresh Cheese Raviolini due to undeclared eggs. The retail unit has the correct label on top, Cheese Raviolini which declares the precense of eggs in the ingredient statement and contains statement. However, the product has the incorrect label on the bottom, Cheese Rigatoni, which does not declare eggs in the ingredient statement or contains statement. The Raviolini label declares: Wheat, Milk, and Eggs whereas the Rigatoni label declares: Wheat and Milk. Since both labels are on the product consumers may be confused as to which ingredients are actually present.

Classification

Class III — A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.

Distribution Pattern

Product was distributed to Whole Foods Markets in the Florida and the NE/NA Region (Massachusetts, Connecticut, Rhode Island, New Hampshire, Maine) Whole Foods Florida DC, 2700 NW 19th Street, Ste 100, Pompano Beach, FL. Whole Foods NE/NA DC, 400 East Johnson Ave, Cheshire, CT. 06410

Product Quantity

42 cases, 378 units were produced

What Should You Do?

Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.

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Frequently Asked Questions

Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.

If you have a food allergy and consumed the recalled product, monitor yourself closely for allergic reaction symptoms — including hives, swelling, difficulty breathing, nausea, vomiting, or anaphylaxis. If you experience any symptoms, seek medical attention immediately. For anaphylaxis (severe allergic reaction with difficulty breathing, rapid heartbeat, or loss of consciousness), call 911 and use an epinephrine auto-injector (EpiPen) if available. Stop consuming the product and check all products from the same manufacturer for similar labeling issues, as undeclared allergens sometimes affect multiple products from the same production facility.

Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.

The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.

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