Preferred Pharmaceuticals is recalling Alprazolam 1mg tablets (30-count and 60-count bottles) due to potential cross-contamination from another product during manufacturing. This recall follows a CGMP deviation by Breckenridge Pharmaceuticals.
CGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc due to potential risk of Cross Contamination.
Preferred Pharmaceuticals is recalling 1mg Alprazolam tablets in 30-count and 60-count bottles because of a potential cross-contamination risk during manufacturing. This could affect people taking these medications, especially those with specific health conditions.
The recall is due to a potential cross-contamination risk during manufacturing at Breckenridge Pharmaceuticals. This means the medication might contain traces of another product, which could be harmful for people with certain health conditions.
People with prescriptions for Alprazolam 1mg tablets who received the recalled bottles from Preferred Pharmaceuticals. Those with specific health conditions that require precise medication may be at higher risk.
Check for 30-count bottles (NDC 68788-7596-3) or 60-count bottles (NDC 68788-7596-6) with expiration dates of 8/31/2024. The product is prescription-only and manufactured by Breckenridge Pharmaceuticals.
Look for the product's NDC number and expiration date on the bottle to confirm if it's part of the recall.
The recall is due to a potential cross-contamination risk during manufacturing at Breckenridge Pharmaceuticals, which could affect people with specific health conditions.
The official notice does not specify a remedy for this recall.
Check for 30-count bottles (NDC 68788-7596-3) or 60-count bottles (NDC 68788-7596-6) with an expiration date of 8/31/2024.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0506-2023 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0506-2023 from Preferred Pharmaceuticals. 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.
