Aonic Complete His. Dosage liquid dietary supplement bottles recalled due to possible coliforms, E. coli, and Pseudomonas aeruginosa contamination. Consumers should check lot numbers and contact the manufacturer for details.
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Aonic Complete His. Dosage liquid dietary supplements are being recalled because they may contain harmful bacteria like E. coli and Pseudomonas aeruginosa. This could cause illness if consumed, so affected consumers should stop using the product.
The product may contain harmful bacteria such as coliforms, E. coli, and Pseudomonas aeruginosa. These bacteria can cause food poisoning if the contaminated product is ingested.
People who purchased the Aonic Complete His. Dosage liquid supplements with lot numbers 5349A BB or 5363A BB from December 27, 2023, are affected. Those who have consumed the product are at risk of foodborne illness.
Check for lot numbers 5349A BB or 5363A BB on the bottle label. The product was sold in two 15-count boxes inside a corrugated Aonic Master Shipper, with the manufacturer address on the label.
Look for lot numbers 5349A BB or 5363A BB on the bottle label.
If you have the recalled product, stop using it immediately to avoid potential illness.
The product may contain harmful bacteria such as coliforms, E. coli, and Pseudomonas aeruginosa, which can cause food poisoning if ingested.
Check for lot numbers 5349A BB or 5363A BB on the bottle label. The product was sold in two 15-count boxes inside a corrugated Aonic Master Shipper.
Stop using the product immediately and contact the manufacturer for further instructions.
We’ve drafted a message you can send Aonic to request your refund or repair — edit it as you like.
Subject: Recall H-0521-2026 — Aonic Aonic Hello, I own a Aonic that is covered by recall H-0521-2026 from Aonic. 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.
