FROZEN PREPARED FOODS 1. FRESH MARKET GLUTEN FREE COMBO PIZZA UPC 737...

FDA Recall #F-1524-2022 — Class II — June 16, 2022

Recall Summary

Recall NumberF-1524-2022
Date InitiatedJune 16, 2022
ClassificationClass II
StatusTerminated
TypeVoluntary: Firm initiated
Product TypeFood

Recalling Firm

FirmUnited Natural Foods, Inc.
LocationChesterfield, NH

Product Description

FROZEN PREPARED FOODS 1. FRESH MARKET GLUTEN FREE COMBO PIZZA UPC 73709421202 12 OZ DI MANUFACTURING 2. FRESH MARKET GLUTEN FREE PEPPERONI PIZZA UPC 73709421016 12 OZ DI MANUFACTURING 3. FRESH MARKET GF MARGHRITA PIZZA UPC 73709421201 12 OZ DI MANUFACTURING 4. ALIVE & KICK PIZZA DOUGH BALL INDVIDUAL BAG UPC 81267001421 23 OZ VISTAR/ VSA 5. ALIVE & KICK PIZZA DOUGH BALL INDVIDUAL BAG UPC 81267001421 23 OZ PERFORMANCE FOOD GRO 6. IMP GARDEN VEG & PORK POTSTICKERS UPC 88012445118 2 LB JYC ENTERPRISE INC 7. IMPERIAL GARDEN VEG & CHKN POTSTICKERS 88012445518 8 2LB JYC ENTERPRISE INC 8. ULTIMO PB 12 IN PIZZA CRUST UPC 80679553175 10 OZ VISTAR/ VSA 9. ULTIMO PB 12 IN PIZZA CRUST UPC 80679553175 10 OZ PERFORMANCE FOOD GRO 10. ULTIMO PB 12 IN PIZZA CRUST UPC 80679553175 10 OZ VISTAR/ VSA 11.ULTIMO PB 12 IN PIZZA CRUST UPC 80679553175 10 OZ PERFORMANCE FOOD GRO 12. JUSROL ROUND & THIN PIZZA CRUST 7.8OZ UPC 6211095547 7.8OZ CERELIA USA BAKERY 13. BAKED GARLIC KNOTS UPC 7648980013 1.3 OZ EUROPASTRY USA INC 14. BAKED GARLIC KNOTS UPC 7648980013 60 1.3 OZ EUROPASTRY USA INC 15. WENNER RND SRDOUGH BREAD UPC 7648907555 19.5 OZ EUROPASTRY USA INC 16. WENNER SRD RSMRY ALP LOAF UPC 7648907369 19.5 OZ EUROPASTRY USA INC 17. WENNER SRD RSMRY ROUND UPC 7648907027 19.5 OZ EUROPASTRY USA INC 18. WENNER FRENCH BAGUETTE BULK 10.5 OZ UPC 7648907071 10.5 OZ EUROPASTRY USA INC 19. WENNER FRENCH BAGUETTE BULK 10.5 OZ UPC 7648907071 10.5 OZ EUROPASTRY USA INC 20. JUSROL PUFF PASTRY 13.2 OZ UPC 6211095550 13.2 OZ CERELIA USA BAKERY

Reason for Recall

Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.

Classification

Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

Distribution Pattern

AL, MS

Product Quantity

N/A

Product Codes / Lot Numbers

various

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.

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.

In most cases, yes. Retailers are typically notified to accept returns of recalled products and issue refunds, regardless of whether you have a receipt. Check with the store where you purchased the item. Some manufacturers also offer direct refunds — contact the recalling firm using the information in the official recall notice. If you purchased the product online, contact the retailer's customer service with your order number. In either case, you generally do not need original packaging, though retaining the product label with the lot code or UPC can speed up the process.

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.