Preferred Pharmaceuticals recalls 30-count 0.25mg Alprazolam tabs (NDC 68788-7594-3, Lot G1822K) due to potential cross-contamination from another product during manufacturing.
CGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc due to potential risk of Cross Contamination.
Preferred Pharmaceuticals is recalling 30-count 0.25mg Alprazolam tabs because of potential cross-contamination during manufacturing. This could affect people taking these medications if they are exposed to other drugs.
The recall is due to potential cross-contamination during manufacturing at Breckenridge Pharmaceuticals, Inc. This means the medication might contain traces of another drug that could cause unintended effects.
People with prescriptions for 0.25mg Alprazolam tabs who received this specific batch (NDC 68788-7594-3, Lot G1822K) are affected. Those with other medications may be at risk if cross-contamination occurred.
Check for the 30-count bottle labeled 'Alprazolam Tab, USP 0.25mg (CIV), Rx Only' with NDC 68788-7594-3 and Lot G1822K. The expiration date is May 31, 2023.
Look for the NDC code 68788-7594-3 and lot number G1822K on the bottle label.
The recall is for potential cross-contamination risk, but the product is not unsafe to use if you don't have the specific lot number mentioned.
Check the bottle label for NDC 68788-7594-3 and lot number G1822K, which expires May 31, 2023.
The recall does not require immediate action; check the product details and contact your healthcare provider if you have concerns.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0504-2023 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0504-2023 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.
