Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Atrapro Antipruritic Hydrogel Recalled by Oculus Innovative Sciences Inc Due to Out of specification result - stability test failure...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Oculus Innovative Sciences Inc directly.
Affected Products
Atrapro Antipruritic Hydrogel, 1.5 oz gel tube, 4 Net wt/ 1.5 oz.. RX only, Professional Sample, Not for Sale. Pre-printed tube: MS31071, Shelf carton: PL51091-08 Atrapro Antipruritic HydroGel is indicated to manage and relieve the burning, itching and pain experienced with various types of dermatoses, including radiation dermatitis and atopic dermatitis.
Quantity: 56,566 1.5 oz tubes
Why Was This Recalled?
Out of specification result - stability test failure of free available chlorine (FAC) which functions as a preservative for the hydrogel. The 13 month test result obtained was 4 ppm FAC and the stability specification is >10 ppm FAC.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Oculus Innovative Sciences Inc
Oculus Innovative Sciences Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report