Colgate Max Fresh Clean Mint 1.9oz Sku 900596 Colgate Cavity…
CGMP Deviations: product held outside appropriate storage temperature conditions.
Yes — there is an active recall. 9 ongoing FDA recalls mention Fluoride (45 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Fluoride. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
CGMP Deviations: product held outside appropriate storage temperature conditions.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Labeling: Not Elsewhere Classified; the primary label (tube) may be incorrectly labeled as Fluoride-Free instead of With Fluoride
Microbial Contamination of Non-Sterile Product
Presence of Foreign Substance: possibility of the presence of metal in the product.
Presence of Foreign Substance; low concentration of an additional flavoring ingredient, Patchouli oil resulting in complaints of off flavor/scent
Label Mix up; rear panel is incorrectly labeled with the PreviDent 5000 Enamel Protect rear panel.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Stability Data Does Not Support Expiry
Labeling:Label Mixup; MULTIVITAMIN/MULTIMINERAL W/FLUORIDE, Chew Tablet, 1 mg (F) may be potentially mislabeled as ISOMETHEPTENE MUCATE/ DICHLORALPHENAZONE/APAP, Capsule, 65 mg/100 mg/325 mg, NDC 44183044001, Pedigree: AD22858_1, EXP: 3/31/2014.
CGMP Deviations: Product was made with an incorrect ingredient, Laureth-9 was mistakenly substituted for PEG.
Free recall alerts
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.