Medline Antifungal Cream Recalled for False Paraben-Free Labeling
Medline Remedy Clinical antifungal cream is recalled for labeling that falsely claims to be paraben-free while the product actually contains parabens. About 1,786 tubes nationwide are affected.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class II labeling issue with no reported illnesses or injuries. The discrepancy between the 'Paraben Free' label claim and the actual paraben content is a minor labeling error consistent with moderate-severity recalls.
Plain-English summary
Medline Industries, LP is recalling Medline Remedy Clinical TREAT Antifungal Cream (2% Miconazole Nitrate) because the product labeling states "Paraben Free" while the formulation actually contains parabens as ingredients.
Approximately 1,786 tubes are affected and were distributed nationwide in the USA. The affected lot numbers are 08926, 08926A (expiring August 2025), and 08928 (expiring September 2025).
Consumers with this product should be aware that the labeling claim does not match the actual formulation. If you have purchased an affected lot and have concerns or questions, contact Medline Industries, LP or consult with a healthcare provider.
The recalled product
- Product
- MEDLINE (MICONAZOLE NITRATE)
- Brand
- MEDLINE
- Manufacturer
- MEDLINE INDUSTRIES, LP - Northfield
- Category
- Drug
- Hazard
- Affected units
- 1,786
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Lot #s: 08926
- 08926A Exp. 8/2025
- 08928 Exp. 9/2025
Distribution
Distributed nationwide across the United States.
Related recalls
Same brand · MEDLINE
- ModerateMedline Remedy Specialized Silicone Cream Recalled for Elevated Formaldehyde Levels
FDA (Drugs) · 2026-07-15
Same manufacturer · MEDLINE INDUSTRIES, LP - Northfield
See all →- CriticalIntubation trays recalled after laryngoscope handle lights failed to illuminate
FDA (Devices) · 2025-10-01
- SevereMedline Medical Convenience Kits with Defective Laryngoscope Handles
FDA (Devices) · 2025-10-01
- HighGood Neighbor alcohol prep pads recalled for alcohol below labeled concentration
FDA (Drugs) · 2025-09-03
- HighSurgical kits recalled because Foley tray inserts carry incorrect product information
FDA (Devices) · 2025-09-03
- HighSurgery trays recalled because they contain recalled tourniquet cuffs
FDA (Devices) · 2025-09-03
Same hazard · mis labeling
See all →- SevereImperio Distribution Recalls Beef Jerky Produced Without Federal Inspection
USDA FSIS · 2026-10-24
- ModerateHealthmark Vinyl Instrument Guards Recalled for Labeling Non-Compliance
FDA (Devices) · 2026-10-21
- ModerateGore Viabil Short Wire Biliary Endoprosthesis Recalled for Incorrect Length Labeling
FDA (Devices) · 2026-10-21
- ModerateIn2bones Recalls Partially Threaded Bone Screws Due to Labeling Error
FDA (Devices) · 2026-10-21
- SevereInstrumentation Laboratory Recalls HemoslL AcuStar HIT-lgG In Vitro Diagnostic Reagents
FDA (Devices) · 2026-10-21
Similar recalls
- ModerateAntifungal Powder Recalled Due to Low Active Ingredient Content
FDA (Drugs) · 2023-11-15
- ModerateMedline Remedy Barrier Ointment Recalled for Microbial Contamination
FDA (Drugs) · 2019-02-13
- ModerateMedline Remedy Specialized Silicone Cream Recalled for Elevated Formaldehyde Levels
FDA (Drugs) · 2026-07-15
- ModerateAntifungal cream recalled over contamination found at the same manufacturing facility
FDA (Drugs) · 2025-11-26
- LowNovartis Recalls Lamisil AT Antifungal Cream Due to Illegible Labeling
FDA (Drugs) · 2013-05-29
- SevereMedline Convenience Kits Recalled for Fungal Contamination Risk
FDA (Devices) · 2026-09-23