SterRx recalls 125 mg per 125 mL DilTIAZem HCl in 5% Dextrose Injection (NDC 70324-951-01) due to lack of sterility assurance. This injectable medication is for prescription use only.
Lack of Assurance of Sterility
SterRx is recalling a specific prescription injection product (DilTIAZem HCl in 5% Dextrose) because it may not be sterile. This could lead to infections if used improperly.
The product lacks assurance of sterility, meaning it might contain harmful bacteria or other contaminants. If injected, this could cause serious infections or other health issues.
Prescription patients who received this specific injection product from SterRx. Healthcare providers using the product for medical treatment are most at risk.
Check for the product name 'DilTIAZem HCl in 5% Dextrose Injection', strength 125 mg per 125 mL, and NDC number 70324-951-01. This product was sold by SterRx in Plattsburgh, NY.
Verify the product name, strength, and NDC number to confirm if it's affected.
The recall states there is a lack of sterility assurance, so it is not safe to use. Do not use this product.
Check for the product name 'DilTIAZem HCl in 5% Dextrose Injection', strength 125 mg per 125 mL, and NDC number 70324-951-01.
The recall does not specify a remedy, so contact your healthcare provider or SterRx directly for guidance.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0315-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0315-2022 from SterRx. 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.
