Comvita branded Manuka Honey + Lion's Mane for Focus recall — FDA H-0014-2025
Leaking induction seal on packaging.
Complete FDA and NHTSA recall records dated in June 2025.
These records include useful source details for the selected month.
Leaking induction seal on packaging.
Cucumbers have the potential to be contaminated with Salmonella
Potential contamination with Salmonella.
Foreign Material (plastic)
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Atlantic Salmon Portions with Seafood Stuffing was incorrectly labeled and does not declare allergen ingredient (SOY)
Leaking induction seal on packaging.
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Cucumbers have the potential to be contaminated with Salmonella
The ingredients statement declares fish sauce but does not declare anchovies. The Contains statement does not declare fish (anchovies).
Foreign Material (plastic)
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Firm's product, Creamy Butter Sauce, was manufactured with recalled ingredient (Cilantro) which contained small wood like pieces.
Potential Salmonella Contamination
Cucumbers have the potential to be contaminated with Salmonella
Cucumbers have the potential to be contaminated with Salmonella
Tesla, Inc. (Tesla) is recalling certain 2026 Model 3 and Model Y vehicles. The fasteners attaching the seat back to the seat bottom may have been improperly tightened.
Failed Impurities/Degradation Specifications: Out of Specification (OOS) for related substances test for Anhydro Simvastatin at the 06-month time point during long-term stability study.
Presence of a foreign substance: black hair found embedded in tablet.
Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was…
Presence of Foreign Tablets/Capsules: manufacturer recalled because one tadalafil 5mg tablet was found in 500 count bottle of Celecoxib 200 mg capsules
Microbial contamination of non-sterile products: tablets may exhibit black spots due to microbial contamination.
Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil 5mg tablet inside a sealed 500-count bottle of Celecoxib 200mg capsule
Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was…
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.