RecallHawk
Class II Recall

WEGMANS STEAM CHOPPED SPINACH 12/12OZ Poly steam bags

NORTERA FOODS USA

Summary

The FDA issued a Class II for WEGMANS STEAM CHOPPED SPINACH 12/12OZ Poly steam bags by NORTERA FOODS USA. Reason: Product may be contaminated with rodent hair and parts.

Details

Source

Food Recall

External ID

F-0745-2023

Action Date

2023-04-26

Status

Terminated

Category

food

Product Description

WEGMANS STEAM CHOPPED SPINACH 12/12OZ Poly steam bags

Lot/Code Info: Daycode: K30247 UPC: 77890 369367 Best if used by: JUL 24 24

Quantity Affected: N/A

Reason for Recall

Product may be contaminated with rodent hair and parts

Distribution

NY

Type: Voluntary: Firm initiated

Recall Initiated: 2023-03-17

Company

NORTERA FOODS USA

Rochester, NY

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 50 food recalls issued in the same week, part of 204 food-related FDA actions this month.

NORTERA FOODS USA has 2 FDA actions in our database, including 2 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 (NORTERA FOODS USA) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does NORTERA FOODS USA have FDA actions?

NORTERA FOODS USA has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0745-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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