CLASS III Drug recall · Reported 4 Oct 2023 · FDA Enforcement Report
Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%) recalled
RB Health (US) is recalling Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%), distributed nationwide in the US. The recall was initiated on 29 Aug 2023 and the FDA has classified it as Class III.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1179-2023
- FDA event ID
- 92977
- Recalling firm
- RB Health (US), Parsippany, NJ
- Manufacturer
- Reckitt Benckiser LLC
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 29 Aug 2023
- FDA classified
- 27 Sep 2023
- Reported
- 4 Oct 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Labeling Errors
Timeline
| 29 Aug 2023 | Recall initiated by company | |
| 27 Sep 2023 | Classified by FDA | +29 days |
| 4 Oct 2023 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.
Product as listed by the FDA
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
Where it was distributed
USA nationwide
Questions about this recall
Is Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%) recalled?
Yes. RB Health (US) recalled Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%) on 29 Aug 2023. The recall is Class III and its status is Terminated. Recall number D-1179-2023.
Why was it recalled?
Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.
Which lots are affected?
Lot # KT220211, Exp 07/2024
Where was it sold?
USA nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other Salicylic Acid recalls
All 4| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Kingskin, Elimina Las Verrugas, For the removal of common warts fl recalledKingskin | Pharmadel | Manufacturing (CGMP) Deviations | DE |
| Drug | CLASS II | Salicylic Acid Solution in all strengths including recalled | Synergy Rx | Sterility | Nationwide |
| Drug | CLASS III | Salicylic Acid Cream recalled by L. Perrigo | L. Perrigo | Potency & Assay | Nationwide |