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