Direct Rx is recalling 0.5 mg Alprazolam C-IV tablets due to potential cross contamination during repackaging. This recall affects specific lots and expiration dates. Consumers should check their product details.
CGMP Deviations: Repackaging firm recalling due to potential product cross contamination concerns at the manufacturer.
Direct Rx is recalling a specific lot of 0.5 mg Alprazolam C-IV tablets because of potential cross contamination during repackaging. This means the medication might have been contaminated with other substances, which could be harmful if taken.
The recall is due to potential cross contamination during repackaging at the manufacturer. This means the medication might have been mixed with other substances, which could be harmful if taken by patients. However, the risk is considered low as it involves potential contamination rather than a direct safety hazard.
People who have the specific lot number 11AP2219 of Direct Rx Alprazolam C-IV tablets (0.5 mg, 30 tabs per bottle) with an expiration date of April 30, 2023. Those who are prescribed this medication and have the affected lot are most at risk.
Check for the lot number 11AP2219 and expiration date of April 30, 2023 on the product label. The product is a 0.5 mg Alprazolam C-IV tablet bottle with 30 tabs per bottle, sold by Direct Rx.
Look for the lot number 11AP2219 and expiration date of April 30, 2023 on the product label.
Direct Rx is recalling this product due to potential cross contamination during repackaging at the manufacturer.
Check the product label for the lot number 11AP2219 and expiration date of April 30, 2023. If you have this specific lot, contact Direct Rx for further instructions.
The recall is due to potential cross contamination, but the risk is considered low. If you have the specific lot number, you should check with Direct Rx for guidance.
We’ve drafted a message you can send Direct Rx to request your refund or repair — edit it as you like.
Subject: Recall D-0507-2023 — Direct Rx Direct Rx Hello, I own a Direct Rx that is covered by recall D-0507-2023 from Direct Rx. 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.
