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Class II: temporary or reversible health riskOngoing

Direct Rx Alprazolam C-IV Recall

Alprazolam C-IV, 0

Direct Rx · Dawsonville, GA

Risk level
Class II
Reported by FDA
Apr 12, 2023
Recall ID
D-0507-2023
Check your lot numberHow we source this data

Summary

Direct Rx recalled Alprazolam C-IV starting Mar 22, 2023. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0507-2023 on Apr 12, 2023. Reason: CGMP Deviations: Repackaging firm recalling due to potential product cross contamination concerns at the manufacturer. Status: Ongoing.

Why it was recalled

CGMP Deviations: Repackaging firm recalling due to potential product cross contamination concerns at the manufacturer.

Product description

Alprazolam C-IV, 0.5 mg, 30 Tabs per bottle, Rx only, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534, NDC 72189-0240-30.

Lot numbers, UPCs & expiration codes

Lot: 11AP2219 Exp. 4/30/23

Where it was sold

Nationwide in the USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0507-2023
Classification
Class II
Status
Ongoing
Recall initiated
Mar 22, 2023
FDA report date
Apr 12, 2023
Quantity
20 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Direct Rx

Original FDA data

Every field from FDA enforcement report D-0507-2023, exactly as published.

Show all FDA fields
City
Dawsonville
State
GA
Status
Ongoing
Country
United States
Event ID
92054
Address
94 Worldwide Dr
Code information
Lot: 11AP2219 Exp. 4/30/23
Postal code
30534-6828
Report date
Apr 12, 2023
Product type
Drugs
Recall number
D-0507-2023
Classification
Class II
Recalling firm
Direct Rx
Product quantity
20 bottles
Reason for recall
CGMP Deviations: Repackaging firm recalling due to potential product cross contamination concerns at the manufacturer.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Alprazolam C-IV, 0.5 mg, 30 Tabs per bottle, Rx only, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534, NDC 72189-0240-30.
Distribution pattern
Nationwide in the USA
Recall initiation date
Mar 22, 2023
Initial firm notification
Letter
Center classification date
Apr 6, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0507-2023, published Apr 12, 2023. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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