45 FDA recalls mention Fluoride. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Fluoride.
Reason CGMP Deviations: product held outside appropriate storage temperature conditions.
Reason CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Reason Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Reason Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Reason Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Reason Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Reason Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Reason Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Reason Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Reason Labeling: Not Elsewhere Classified; the primary label (tube) may be incorrectly labeled as Fluoride-Free instead of With Fluoride
Reason Microbial Contamination of Non-Sterile Product
Reason Presence of Foreign Substance: possibility of the presence of metal in the product.
Reason Presence of Foreign Substance; low concentration of an additional flavoring ingredient, Patchouli oil resulting in complaints of off flavor/scent
Reason Label Mix up; rear panel is incorrectly labeled with the PreviDent 5000 Enamel Protect rear panel.
Reason Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Reason Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Reason Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Reason Stability Data Does Not Support Expiry
Reason Labeling:Label Mixup; MULTIVITAMIN/MULTIMINERAL W/FLUORIDE, Chew Tablet, 1 mg (F) may be potentially mislabeled as ISOMETHEPTENE MUCATE/…
Reason CGMP Deviations: Product was made with an incorrect ingredient, Laureth-9 was mistakenly substituted for PEG.
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