Clearasil Rapid Rescue Deep Treatment Pads recall: Labeling Error
Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%), packaged in 90-count plastic jar, further packaged in case of 6 jars per case, Distributed by RB Health (US), Parsippany, NJ 07054, NDC 63824-431-90
Why was Clearasil Rapid Rescue Deep Treatment Pads recalled?
Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.
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 # KT220211, Exp 07/2024
- Product
- Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%), packaged in 90-count plastic jar, further packaged in case of 6 jars per case, Distributed by RB Health (US), Parsippany, NJ 07054, NDC 63824-431-90
- Recalling firm
- RB Health (US) LLC
- Quantity
- 6,072 cases/36,426 individual selling units
- Distribution
- USA nationwide
- Recall date
- October 4, 2023
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)