FDA recall record

Comvita branded Manuka Honey + Lion's Mane for Focus recall — FDA H-0014-2025

Leaking induction seal on packaging.

Class IIclassification
H-0014-2025official record ID
Jun 18, 2025report date

Recall record at a glance

Official recordH-0014-2025
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCOMVITA USA Inc.
Report dateJun 18, 2025
Recall initiation dateMay 23, 2025
Quantity2,730 units
LocationSanta Barbara, CA, United States

Official product description

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

Why the product was recalled

Leaking induction seal on packaging.

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.