Breckenridge Pharmaceutical recalls 0.5mg Alprazolam tablets due to potential cross contamination. Affected lots have specific NDC numbers and expiration dates. Consumers should check their product details.
CGMP Deviations: Potential risk of Cross Contamination
Breckenridge Pharmaceutical is recalling 0.5mg Alprazolam tablets that may have cross contamination risks. This recall affects specific packaging sizes and expiration dates. If you have these products, you should check if they match the listed lots and expiration dates.
The recall is due to potential cross contamination during manufacturing. This means the medication might contain other substances that could be harmful, though the exact risk level is not specified in the notice.
People who have the recalled 0.5mg Alprazolam tablets in 100-count, 500-count, or 1,000-count bottles with the listed NDC numbers and expiration dates. Prescriptions for these medications are at risk of cross contamination.
Check for the product name 'Alprazolam Tablets, USP, 0.5mg, CIV' in 100-count, 500-count, or 1,000-count bottles with the specific NDC numbers and expiration dates listed in the recall notice.
Look for the NDC numbers 51991-0705-01, 51991-0705-05, or 51991-0705-10 and expiration dates matching the listed lots.
The recall states there is a potential risk of cross contamination, but the exact nature of the contamination is not specified in the notice.
Check the product label for the NDC numbers 51991-0705-01, 51991-0705-05, or 51991-0705-10 and expiration dates listed in the recall notice.
The recall does not specify a stop-use instruction, so you do not need to stop using them immediately. However, you should check if your product matches the affected lots.
We’ve drafted a message you can send Breckenridge to request your refund or repair — edit it as you like.
Subject: Recall D-0459-2023 — Breckenridge Breckenridge Hello, I own a Breckenridge that is covered by recall D-0459-2023 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.
