PreviDent 5000 ppm recall: Labeling Error
PreviDent 5000 ppm, DRY MOUTH, 1.1% Sodium Fluoride, PRESCRIPTION STRENGTH TOOTHPASTE, SLS Free Formula, SOOTHING MINT, 3.4 FL OZ (100 mL), Colgate…
Why was PreviDent 5000 ppm recalled?
Label Mix up; rear panel is incorrectly labeled with the PreviDent 5000 Enamel Protect rear panel.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lots: 6350US561G, 6350US562G, 6351US561G, 6351US562G
- Product
- PreviDent 5000 ppm, DRY MOUTH, 1.1% Sodium Fluoride, PRESCRIPTION STRENGTH TOOTHPASTE, SLS Free Formula, SOOTHING MINT, 3.4 FL OZ (100 mL), Colgate…
- Recalling firm
- Colgate Palmolive Co
- Quantity
- 14,656 bottles
- Distribution
- Nationwide
- Recall date
- March 22, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)