Homeocare Laboratories recalls SnoreStop Naso Spray due to cGMP deviations. This may affect product safety and quality. Consumers should check their product's lot number.
cGMP deviations
Homeocare Laboratories is recalling SnoreStop Naso Spray bulk liquid product due to cGMP deviations. This recall affects product safety and quality, though specific risks aren't detailed in the notice.
cGMP deviations refer to failures in manufacturing quality standards that could lead to unsafe products. This means the SnoreStop Naso Spray might not meet the required safety and quality levels for consumer use.
People who purchased SnoreStop Naso Spray from Green Pharma with NDC 61152-199-99 are likely affected. Those using the product for snoring relief may be at risk if the product was made without proper quality controls.
Check for the product name 'SnoreStop Naso Spray', distributed by Green Pharma, with NDC code 61152-199-99. The lot number is 2436, but the expiration date is unknown.
Identify the product by its NDC code 61152-199-99 and lot number 2436.
The recall is due to cGMP deviations, which may affect product safety and quality, but specific risks aren't detailed in the notice.
Check for the NDC code 61152-199-99 and lot number 2436 on the product label.
The recall notice does not specify a remedy, so no action is required beyond checking if you have the product.
We’ve drafted a message you can send Homeocare to request your refund or repair — edit it as you like.
Subject: Recall D-0885-2023 — Homeocare Homeocare Hello, I own a Homeocare that is covered by recall D-0885-2023 from Homeocare. 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.
