Kenil Healthcare recalls Rapidol Maximum Strength Hydrocortisone 1% Anti-Itch Cream due to CGMP deviations. Consumers should check product details and contact the manufacturer for instructions.
CGMP Deviations
Kenil Healthcare is recalling Rapidol Maximum Strength Hydrocortisone 1% Anti-Itch Cream tubes because of manufacturing quality control issues. This recall affects products distributed by Pharmadel LLC with specific lot numbers and expiration dates.
CGMP deviations refer to manufacturing quality control issues that could affect product safety and effectiveness. These deviations may lead to potential product contamination or improper formulation, though the exact risk is not specified in the recall notice.
People who own or use the Rapidol Maximum Strength Hydrocortisone 1% Anti-Itch Cream tubes distributed by Pharmadel LLC are affected. Those with the specific lot number SP26A and expiration date 09/30/2026 are most at risk.
Check for the product name 'Rapidol Maximum Strength Hydrocortisone 1% Anti-Itch Cream', net weight 2 oz (60g) tube, distributed by Pharmadel LLC. Look for lot number SP26A and expiration date 09/30/2026.
Identify the product by checking the label for the lot number SP26A and expiration date 09/30/2026.
The recall notice states there are CGMP deviations, but does not specify if the product is safe to use. Consumers should contact the manufacturer for instructions.
The recall notice does not provide a remedy, so consumers should check the product details and contact Kenil Healthcare for further instructions.
Check the product label for lot number SP26A and expiration date 09/30/2026. If these match, the product is recalled.
We’ve drafted a message you can send Kenil Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0428-2025 — Kenil Healthcare Kenil Healthcare Hello, I own a Kenil Healthcare that is covered by recall D-0428-2025 from Kenil Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
