SterRx recalls 125mg/125mL dilTIAZem HCl injection (NDC 70324-976-01) due to lack of sterility assurance. This Rx-only medication may cause infections if used.
Lack of Assurance of Sterility
SterRx is recalling a specific injection medication because it may not be sterile. Using this product could lead to infections, especially since it's a prescription drug.
The injection lacks proper sterility assurance, meaning it could contain harmful bacteria or other contaminants. This poses a risk of infection if the medication is administered.
Prescription patients who received this specific injection from SterRx in New York. Those with the NDC 70324-976-01 lot numbers listed are most at risk.
Check the product label for the NDC 70324-976-01 code and lot numbers S21164/BTV through S21300/BYQ. This medication was sold in New York starting December 2021.
Look for the NDC code 70324-976-01 and lot numbers S21164/BTV through S21300/BYQ on the injection bottle.
The recall states there is a lack of sterility assurance, so it may not be safe. Do not use this product until the recall is resolved.
The recall does not specify a remedy, so contact SterRx directly for guidance on safe disposal or alternatives.
Check the product label for the NDC 70324-976-01 and lot numbers S21164/BTV through S21300/BYQ.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0302-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0302-2022 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.
