On May 23, 2025, Comvita, a California-based company known for its specialty manuka honey, voluntarily recalled three of its honey formulations due to faulty packaging. Specifically, the induction seals—a critical safety component placed under the lid—were improperly applied. This has led to product leakage and possible tampering concerns.
The FDA announced the classification of the recall on June 9, 2025, stating the issue could potentially cause temporary or medically reversible adverse health effects, but that the probability of serious health consequences remains low.
The recall involves the following 355g Comvita Manuka Honey products:
Manuka Honey + Lion’s Mane (Focus)
Lot Codes: 34828522, 34835584
Expiration Dates: January 21, 2026 & February 21, 2026
Manuka Honey + Cordyceps (Energy)
Lot Codes: 34828523, 34835585
Expiration Dates: January 22, 2026 & February 25, 2026
Manuka Honey + Reishi (Wellness)
Lot Codes: 34828521, 34835574
Expiration Dates: January 21, 2026 & February 24, 2026
A total of 2,730 units of each variant were sold across the following states:
Packaging integrity is a critical component of food safety assurance. According to Professor Byron Chaves, a food safety expert at the University of Nebraska-Lincoln:
“Induction seals provide a tamper-evident, air-tight barrier that maintains product freshness and prevents contamination. If these seals are compromised, there is a risk of leakage and potential microbial exposure, which undermines consumer trust and regulatory compliance.”
While no illnesses have been reported as of June 9, the FDA and Comvita have taken a proactive approach by classifying the issue and initiating the recall swiftly.
Consumers are strongly advised not to consume the affected honey products. Instead, they should:
Check product labels for the lot codes and expiration dates listed above.
Return affected units to the place of purchase for a full refund.
Dispose of leaking containers safely, as improper sealing may also lead to reduced shelf life and contamination risk.
Retailers are instructed to remove the affected stock from shelves immediately and inform customers of the recall.
Source: Newsweek & FDA