Breckenridge Pharmaceutical recalls 0.25mg Alprazolam tablets due to potential cross contamination from manufacturing. Affected lots include specific NDC numbers and expiration dates. Consumers should check their product details.
CGMP Deviations: Potential risk of Cross Contamination
Breckenridge Pharmaceutical is recalling 0.25mg Alprazolam tablets that may have been contaminated during manufacturing. This recall affects specific packaging sizes and lot numbers with potential cross contamination risks.
The recall is for potential cross contamination during manufacturing, which could mean the medication is mixed with other substances. This might affect the safety and effectiveness of the drug, but the risk is not described as causing serious injury or death.
People who have the 0.25mg Alprazolam tablets in 100-count, 500-count, or 1,000-count bottles with specific lot numbers and expiration dates. Those using prescription-only medications for anxiety or related conditions are most at risk.
Check for 100-count, 500-count, or 1,000-count bottles labeled with NDC 51991-0704-01 or specific lot numbers like 5210734 through 5211271. The expiration dates range from April 30, 2023, to July 31, 2024.
Look for the NDC number 51991-0704-01 on the 100-count bottle or specific lot numbers listed in the recall notice.
The recall is due to potential cross contamination during manufacturing, which could affect the safety and effectiveness of the medication.
Check the product details to see if your medication is affected. If it is, contact your healthcare provider for advice.
Yes, specific lot numbers from 5210734 to 5211271 are affected, with expiration dates ranging from April 30, 2023, to July 31, 2024.
We’ve drafted a message you can send Breckenridge to request your refund or repair — edit it as you like.
Subject: Recall D-0458-2023 — Breckenridge Breckenridge Hello, I own a Breckenridge that is covered by recall D-0458-2023 from Breckenridge. 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.
