RecallHawk
Class II Recall

Comvita branded Manuka Honey + Lion's Mane for Focus; made in New Zealand, Net Wt. 12 fl oz (355g); Barcode# 65819600102

COMVITA USA INC

Summary

The FDA issued a Class II for Comvita branded Manuka Honey + Lion's Mane for Focus; made in New Zealand, Net W by COMVITA USA INC. Reason: Leaking induction seal on packaging..

Details

Source

Food Recall

External ID

H-0014-2025

Action Date

2025-06-18

Status

Terminated

Category

food

Product Description

Comvita branded Manuka Honey + Lion's Mane for Focus; made in New Zealand, Net Wt. 12 fl oz (355g); Barcode# 658196001020

Lot/Code Info: Lot# 34828522; Best By date: Jan/21/2026 Lot# 34835584; Best By date: Feb21/2026

Quantity Affected: 2,730 units

Reason for Recall

Leaking induction seal on packaging.

Distribution

Distribution centers are located in CO, AZ, TX, MD, FL, CA, GA.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-23

Company

COMVITA USA INC

Santa Barbara, CA

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

COMVITA USA INC has 3 FDA actions in our database, including 3 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 (COMVITA USA INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does COMVITA USA INC have FDA actions?

COMVITA USA INC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0014-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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