Preferred Pharmaceuticals recalls Alprazolam 1mg tablets (NDCs 68788-6381-03, 06, 09) for CGMP deviations. Consumers should check lot numbers and expiration dates on packaging.
CGMP deviations
Preferred Pharmaceuticals is recalling certain Xanax 1mg tablets due to manufacturing deviations. This recall is important because the issue could affect product safety and quality.
The recall is for CGMP (Current Good Manufacturing Practice) deviations, which means the tablets were produced without following standard safety and quality procedures. This could lead to potential product safety issues, though the exact risk is not specified in the recall notice.
People who own or use the recalled Xanax tablets (30, 60, or 90 tablet bottles) are affected. Those with the specific lot numbers and expiration dates listed are at risk.
Check the product packaging for the NDC codes: 68788-6381-03 (30 tablets), 68788-6381-06 (60 tablets), or 68788-6381-09 (90 tablets). Also look for the lot numbers and expiration date (03/31/2022) on the bottle.
Look for the NDC codes and lot numbers on the packaging to confirm if the product is recalled.
The recall is due to CGMP deviations, which means the tablets were produced without following standard safety and quality procedures.
The recalled products are Alprazolam 1mg tablets in bottles of 30, 60, or 90 tablets with specific NDC codes and lot numbers.
Check the packaging for NDC codes 68788-6381-03, 68788-6381-06, or 68788-6381-09, and lot numbers like G2919M, H3019Q, or F1219N.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0642-2022 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0642-2022 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.
