RecallHawk
Class II Recall

Full Spectrum Cold Pressed Hemp Oil Gummies, Peach, 1.41 oz (4-count) and 8oz (15-count).

Tay's Sales and Distribution

Summary

The FDA issued a Class II for Full Spectrum Cold Pressed Hemp Oil Gummies, Peach, 1.41 oz (4-count) and 8oz ( by Tay's Sales and Distribution. Reason: Sub-ingredients not declared for sunflower butter..

Details

Source

Food Recall

External ID

F-0416-2024

Action Date

2023-11-22

Status

Completed

Category

food

Product Description

Full Spectrum Cold Pressed Hemp Oil Gummies, Peach, 1.41 oz (4-count) and 8oz (15-count).

Lot/Code Info: Lot: 081321 Best by date: 08/23

Quantity Affected: 1.4oz x 50-units, 8oz x 40-units

Reason for Recall

Sub-ingredients not declared for sunflower butter.

Distribution

Direct to consumer and retail establishments in IA and IL.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-03-29

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

Tay's Sales and Distribution has 5 FDA actions in our database, including 5 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 (Tay's Sales and Distribution) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Tay's Sales and Distribution have FDA actions?

Tay's Sales and Distribution has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0416-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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