RecallHawk
Class II Recall

Wegmans brand Roasted Garlic hummus; NET WT 32 OZ (2 LB) 908 g; packaged in clear plastic container with a clear plastic

Wegmans Food Markets, Inc.

Summary

The FDA issued a Class II for Wegmans brand Roasted Garlic hummus; NET WT 32 OZ (2 LB) 908 g; packaged in clea by Wegmans Food Markets, Inc.. Reason: Product may potentially contain blue plastic pieces..

Details

Source

Food Recall

External ID

F-0808-2022

Action Date

2022-03-09

Status

Terminated

Category

food

Product Description

Wegmans brand Roasted Garlic hummus; NET WT 32 OZ (2 LB) 908 g; packaged in clear plastic container with a clear plastic snap lid; Keep Refrigerated

Lot/Code Info: UPC 0-77890-26225-2 Lot #220299 Best By 03/26/22

Reason for Recall

Product may potentially contain blue plastic pieces.

Distribution

MD, MA, NJ, NY, NC, PA, VA

Type: Voluntary: Firm initiated

Recall Initiated: 2022-02-18

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 70 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Wegmans Food Markets, Inc. has 28 FDA actions in our database, including 28 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Wegmans Food Markets, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Wegmans Food Markets, Inc. have FDA actions?

Wegmans Food Markets, Inc. has 28 FDA actions in our database, including 28 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0808-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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