activator concentrate recall: CGMP Deviations
activator concentrate, Sodium Fluoride 0.96% in Activator Concentrate; 0.08% in diluted Activator Solution, Net 1 FL. OZ., Manufactured for: All USA…
Why was activator concentrate recalled?
CGMP Deviations: Products not manufactured under current good manufacturing practices.
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?
Lot: 1E175B, exp 6/24
- Product
- activator concentrate, Sodium Fluoride 0.96% in Activator Concentrate; 0.08% in diluted Activator Solution, Net 1 FL. OZ., Manufactured for: All USA…
- Recalling firm
- Ecometics, Inc.
- Quantity
- 32,583 bottles
- Distribution
- Nationwide in the USA
- Recall date
- August 30, 2023
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (drug)