Washington Homeopathic Products recalls specific Influenzinum liquid pellets due to cGMP deviations. Affected lots include 28960, 28962, 28961, 27415, 27464. Consumers should contact the company for details.
cGMP deviations
Washington Homeopathic Products is recalling certain Influenzinum liquid pellets due to manufacturing quality issues. This recall affects specific lots that may not meet safety standards, though the exact risk is not clearly described.
The recall mentions cGMP deviations, which are regulatory standards for manufacturing quality. However, the record does not specify what these deviations are or how they could affect product safety. Without clear details, the exact hazard mechanism is unknown.
People who purchased Influenzinum liquid pellets from Washington Homeopathic Products in the specified lots are affected. Those using these products for immune support may be at risk if the manufacturing deviations impact safety.
Check the lot numbers on the product label: 28960, 28962, 28961, 27415, or 27464. These liquid pellets are sold as OTC homeopathic remedies by Washington Homeopathic Products.
Look for lot numbers 28960, 28962, 28961, 27415, or 27464 on the label.
The recall is due to cGMP deviations, but the specific nature of the deviations and their impact on safety is not clearly described in the record.
The official notice does not provide a remedy or action steps beyond checking the lot number. Contact Washington Homeopathic Products for further instructions.
The record does not specify any safety risks or injuries, so the exact hazard is unknown.
We’ve drafted a message you can send Washington Homeopathic to request your refund or repair — edit it as you like.
Subject: Recall D-1131-2022 — Washington Homeopathic Washington Homeopathic Hello, I own a Washington Homeopathic that is covered by recall D-1131-2022 from Washington Homeopathic. 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.
