Cardinal Health recalls HySept Solution 0.25% Sodium Hypochlorite Solution 473mL (16 fl oz) manufactured between Feb 2021 and March 2021 due to temperature storage deviations. No remedy provided in official recall.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Cardinal Health is recalling HySept Solution 0.25% Sodium Hypochlorite Solution (473mL) produced between February and March 2021 because of temperature storage issues that could affect product stability. This recall does not include a remedy or return process as stated in the official notice.
The product was exposed to temperature fluctuations during storage, which could lead to instability in the solution. This might affect the product's effectiveness as a disinfectant, though the recall does not specify any immediate safety risks.
People who purchased this specific solution from the manufacturer between February 23, 2021 and March 10, 2021 are affected. The risk is highest for those using the product for disinfection purposes.
Check for the product name 'HySept Solution 0.25% Sodium Hypochlorite Solution 473 mL (16 fl. oz.)' with NDC 39328-063-25. The product was manufactured between February 23, 2021 and March 10, 2021.
Verify the product name, NDC code, and manufacturing dates to confirm if it's part of this recall.
The official recall notice does not provide any remedy or return process.
The product was exposed to temperature fluctuations during storage, which could affect its stability.
The product was manufactured between February 23, 2021 and March 10, 2021.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall D-0540-2021 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall D-0540-2021 from Cardinal Health. 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.
