RecallHawk
Class II Recall

TK006 Van Krimpet Powder Blend 50#. Item number 4107780

Puratos Corporation (HQ and Innovation Center)

Summary

The FDA issued a Class II for TK006 Van Krimpet Powder Blend 50#. Item number 4107780 by Puratos Corporation (HQ and Innovation Center). Reason: Product may be contaminated with foreign material (metal).

Details

Source

Food Recall

External ID

F-0248-2022

Action Date

2021-12-08

Status

Terminated

Category

food

Product Description

TK006 Van Krimpet Powder Blend 50#. Item number 4107780

Lot/Code Info: Batch Numbers 0010636568 and 1110644921,

Quantity Affected: 30,350 lbs

Reason for Recall

Product may be contaminated with foreign material (metal)

Distribution

Distributed to domestic customers in CA, NJ, IN, PA, TN, NY, NC, TX, FL, DE, LA, and LA. Distributed to foreign customers in Dominican Republic and Trinidad.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-10-29

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

Puratos Corporation (HQ and Innovation Center) has 20 FDA actions in our database, including 20 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 (Puratos Corporation (HQ and Innovation Center)) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Puratos Corporation (HQ and Innovation Center) have FDA actions?

Puratos Corporation (HQ and Innovation Center) has 20 FDA actions in our database, including 20 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0248-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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