RecallHawk
Class II Recall

Mott s no sugar added applesauce 6 pack 3.9 oz (111g) Containers 23.4 oz (666g). Individual units are packaged in plasti

MOTTS LLP

Summary

The FDA issued a Class II for Mott s no sugar added applesauce 6 pack 3.9 oz (111g) Containers 23.4 oz (666g). by MOTTS LLP. Reason: Elevated patulin levels.

Details

Source

Food Recall

External ID

F-1016-2023

Action Date

2023-07-05

Status

Terminated

Category

food

Product Description

Mott s no sugar added applesauce 6 pack 3.9 oz (111g) Containers 23.4 oz (666g). Individual units are packaged in plastic cups and placed in a cardboard sleeve of 6 sups with 12 sleeves to a case. Retail unit UPC is 14800000078 . Case label UPC is 10014800000075

Lot/Code Info: 042123LYtt:tt / Best By: AUG 13 24 and 042223LYttt:tt / Best By: AUG 14 24

Quantity Affected: 9,593 cases

Reason for Recall

Elevated patulin levels

Distribution

US states including: AL, CT, FL, GA, IA, IL, IN, KY, MA, MD, ME, MI, MN, MO, NC, NJ, NY, OH, PA, SC, TN, TX, VA, WI; Bermuda and Dominican Republic

Type: Voluntary: Firm initiated

Recall Initiated: 2023-05-18

Company

MOTTS LLP

Frisco, TX

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

MOTTS LLP 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 (MOTTS LLP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does MOTTS LLP have FDA actions?

MOTTS LLP 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-1016-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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