Kenil Healthcare recalls Kofal Athletes Penetrating Pain Relief Ointment due to CGMP deviations. This external analgesic may not meet quality standards. Consumers should check product details and contact the manufacturer for instructions.
CGMP Deviations
Kenil Healthcare is recalling Kofal Athletes Penetrating Pain Relief Ointment (methyl salicylate 10.5%) because of manufacturing quality issues. This recall affects products distributed by Pharmadel LLC with specific lot and expiration dates. The issue could lead to product quality problems, but serious injury risks are not described.
CGMP deviations refer to failures in the manufacturing process that could affect product quality. This means the ointment might not meet safety and quality standards, potentially causing issues for users. However, the recall does not specify serious injury risks.
Anyone who owns or uses the Kofal Athletes Penetrating Pain Relief Ointment with the specified lot number (SP30A) and expiration date (09/30/2026) is affected. People using this product for pain relief are most at risk due to potential quality issues.
Check for the product name 'Kofal Athletes Penetrating Pain Relief Ointment' with methyl salicylate 10.5% concentration. The lot number should be SP30A and the expiration date 09/30/2026. The product was distributed by Pharmadel LLC.
Look for the lot number SP30A and expiration date 09/30/2026 on the product label.
The recall states there were CGMP deviations, which could affect product quality, but serious injury risks are not described.
Check for the lot number SP30A and expiration date 09/30/2026 on the Kofal Athletes Penetrating Pain Relief Ointment label.
The recall does not specify a remedy, so contact Kenil Healthcare directly for instructions.
We’ve drafted a message you can send Kenil Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0426-2025 — Kenil Healthcare Kenil Healthcare Hello, I own a Kenil Healthcare that is covered by recall D-0426-2025 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.
